Massachusetts 2023-2024 Regular Session

Massachusetts Senate Bill S2871 Latest Draft

Bill / Introduced Version Filed 07/15/2024

                            SENATE . . . . . . . . . . . . . . No. 2871
The Commonwealth of Massachusetts
_______________
In the One Hundred and Ninety-Third General Court
(2023-2024)
_______________
SENATE, July 15, 2024.
The committee on Senate Ways and Means to whom was referred the House Bill 
enhancing the market review process (House, No. 4653); reports, recommending that the same 
ought to pass with an amendment striking out all after the enacting clause and inserting in place 
thereof the text of Senate document numbered 2871; and by striking out the title and inserting in 
place thereof the following title "An Act enhancing the health care market review process".
For the committee,
Michael J. Rodrigues 2 of 119
SENATE . . . . . . . . . . . . . . No. 2871
The Commonwealth of Massachusetts
_______________
In the One Hundred and Ninety-Third General Court
(2023-2024)
_______________
1 SECTION 1. Section 16 of chapter 6A of the General Laws, as appearing in the 2022 
2Official Edition, is hereby amended by striking out, in lines 24 to 26, inclusive, the words “, the 
3division of medical assistance and the Betsy Lehman center for patient safety and medical error 
4reduction” and inserting in place thereof the following words:- and the division of medical 
5assistance.
6 SECTION 2. Section 16D of said chapter 6A, as so appearing, is hereby amended by 
7striking out, in lines 22 to 24, inclusive, the words “department of public health established by 
8section 217 of chapter 111” and inserting in place thereof the following words:- health policy 
9commission established by section 16 of chapter 6D.
10 SECTION 3. Section 16N of said chapter 6A is hereby repealed.
11 SECTION 4. Section 16T of said chapter 6A is hereby repealed.
12 SECTION 5. Section 1 of chapter 6D of the General Laws, as so appearing, is hereby 
13amended by inserting after the definition of “Alternative payment methodologies or methods” 
14the following definition:-  3 of 119
15 “Benchmark cycle”, a period of 2 consecutive calendar years during which the projected 
16annualized growth rate in total health care expenditures in the commonwealth is calculated 
17pursuant to section 9 and monitored pursuant to section 10. 
18 SECTION 6. Said section 1 of said chapter 6D, as so appearing, is hereby further 
19amended by inserting after the definition of “Fee-for-service” the following definition:-
20 “Financial interest”, when a private equity firm or its corporate affiliate has a direct or 
21indirect ownership share of, or controlling interest in, or is a holder of significant debt from a 
22provider or provider organization or the provider or provider organization’s corporate affiliates.
23 SECTION 7. Said section 1 of said chapter 6D, as so appearing, is hereby further 
24amended by striking out the definition of “Health care cost growth benchmark” and inserting in 
25place thereof the following definition:-
26 “Health care cost growth benchmark”, the projected annualized growth rate in total health 
27care expenditures in the commonwealth during a benchmark cycle, as established in section 9.
28 SECTION 8. Said section 1 of said chapter 6D, as so appearing, is hereby further 
29amended by inserting after the definition of “Health care provider” the following definition:-
30 “Health care resource”, any resource, whether personal or institutional in nature and 
31whether owned or operated by any person, the commonwealth or political subdivision thereof, 
32the principal purpose of which is to provide, or facilitate the provision of, services for the 
33prevention, detection, diagnosis or treatment of those physical and mental conditions 
34experienced by humans which usually are the result of, or result in, disease, injury, deformity or  4 of 119
35pain; provided, that the term “treatment” shall include custodial and rehabilitative care incident 
36to infirmity, developmental disability or old age.
37 SECTION 9. Said section 1 of said chapter 6D, as so appearing, is hereby further 
38amended by inserting after the definition of “Health care services” the following 2 definitions:-
39 “Health disparities”, preventable differences in the burden of disease, injury, violence or 
40opportunities to achieve optimal health that are experienced by socially disadvantaged 
41populations. 
42 “Health equity”, the state in which a health system offers the infrastructure, facilities, 
43services, geographic coverage, affordability and all other relevant features, conditions and 
44capabilities to provide every resident of the commonwealth with the opportunity and reasonable 
45expectation to achieve optimal health and equal access to health care regardless of race, 
46ethnicity, language, disability, age, gender, gender identity, sexual orientation, social class, 
47intersections among such communities or identities or socially determined circumstances.
48 SECTION 10. Said section 1 of said chapter 6D, as so appearing, is hereby further 
49amended by inserting after the definition of “Hospital service corporation” the following 2 
50definitions:- 
51 “Management services organization”, a corporation that provides management or 
52administrative services to a provider or provider organization for compensation.
53 “Maximum adjusted debt to adjusted EBITDA ratio”, the highest ratio of total adjusted 
54debt to adjusted earnings before interest, taxes, depreciation and amortization the commission 
55determines that a provider or provider organization is permitted to have without becoming  5 of 119
56financially unstable; provided, however, that the commission, in consultation with the center, 
57shall establish a standard method of calculating and reporting total adjusted debt and adjusted 
58earnings before interest, taxes, depreciation and amortization; and provided further, that the 
59methodology and reporting shall include capitalized lease obligations.
60 SECTION 11. Said section 1 of said chapter 6D, as so appearing, is hereby further 
61amended by striking out, in line 189, the words “not include excludes ERISA plans” and 
62inserting in place thereof the following words:- include self-insured plans to the extent allowed 
63under the federal Employee Retirement Income Security Act of 1974.
64 SECTION 12. Said section 1 of said chapter 6D, as so appearing, is hereby further 
65amended by inserting after the definition of “Performance penalty” the following 2 definitions:-
66 “Pharmaceutical manufacturing company”, an entity engaged in the: (i) production, 
67preparation, propagation, compounding, conversion or processing of prescription drugs, directly 
68or indirectly, by extraction from substances of natural origin, independently by means of 
69chemical synthesis or by a combination of extraction and chemical synthesis; or (ii) packaging, 
70repackaging, labeling, relabeling or distribution of prescription drugs; provided, however, that 
71pharmaceutical manufacturing company shall not include a wholesale drug distributor licensed 
72under section 36B of chapter 112 or a retail pharmacist registered under section 39 of said 
73chapter 112.
74 “Pharmacy benefit manager”, a person, business or other entity, however organized, that 
75directly or through a subsidiary provides pharmacy benefit management services for prescription 
76drugs and devices on behalf of a health benefit plan sponsor including, but not limited to, a self-
77insurance plan, labor union or other third-party payer; provided, however, that pharmacy benefit  6 of 119
78management services shall include, but not be limited to: (i) the processing and payment of 
79claims for prescription drugs; (ii) the performance of drug utilization review; (iii) the processing 
80of drug prior authorization requests; (iv) pharmacy contracting; (v) the adjudication of appeals or 
81grievances related to prescription drug coverage contracts; (vi) formulary administration; (vii) 
82drug benefit design; (viii) mail and specialty drug pharmacy services; (ix) cost containment; (x) 
83clinical, safety and adherence programs for pharmacy services; and (xi) management of the cost 
84of covered prescription drugs; provided further, that pharmacy benefit manager shall include a 
85health benefit plan sponsor that does not contract with a pharmacy benefit manager and manages 
86its own prescription drug benefits unless specifically exempted by the commission.
87 SECTION 13. Said section 1 of said chapter 6D, as so appearing, is hereby further 
88amended by inserting after the definition of “Primary care provider” the following definition:-
89 “Private equity firm”, a publicly traded or non-publicly traded company that collects 
90capital investments from individuals or entities and purchases, as a parent company or through 
91another entity that it completely or partially owns or controls, a direct or indirect ownership share 
92of, or controlling interest in, or otherwise obtains a financial interest in, a provider, provider 
93organization or management services organization; provided, however, that private equity firm 
94shall not include venture capital firms exclusively funding startups or other early-stage business.
95 SECTION 14. Said section 1 of said chapter 6D, as so appearing, is hereby further 
96amended by striking out the definition of “Provider organization” and inserting the following 2 
97definitions:-
98 “Provider organization”, a corporation, partnership, business trust, association or 
99organized group of persons that is in the business of health care delivery or management,  7 of 119
100whether incorporated or not that represents 1 or more 	health care providers in contracting with 
101carriers, third party administrators or public payers for the payments of health care services; 
102provided, however, that “provider organization” shall include, but not be limited to, physician 
103organizations, physician-hospital organizations, management services organizations, independent 
104practice associations, provider networks, accountable 	care organizations, providers that are 
105owned or controlled, fully or partially, by for-profit entities including, but not limited to, private 
106equity firms, and any other organization that contracts with carriers, third party administrators or 
107public payers for payment for health care services; and provided further, that “provider 
108organization” shall not include any integrated care network that is owned and directed by long-
109term care.
110 SECTION 15. Said section 1 of said chapter 6D, as so appearing, is hereby further 
111amended by inserting after the definition of “Quality measure” the following definition:-
112 “Real estate investment trust”, a real estate investment trust as defined in 26 U.S.C. 856.
113 SECTION 16. Said section 1 of said chapter 6D, as so appearing, is hereby further 
114amended by inserting after the definition of “Total health care expenditures” the following 2 
115definitions:-
116 “Total medical expenses”, the total cost of care for the patient population associated with 
117a provider organization based on allowed claims for all categories of medical expenses and all 
118non-claims related payments to providers.
119 “Unsafe financial actor”, a private equity firm, private equity firm affiliate or real estate 
120investment trust that has a financial interest in a provider or provider organization closing, 
121declaring bankruptcy, or otherwise discontinuing its operations, within 15 years of the private  8 of 119
122equity firm or real estate investment trust’s financial interest in the provider or provider 
123organization. 
124 SECTION 17. Section 2 of said chapter 6D, as so appearing, is hereby amended by 
125striking out subsections (b) and (c) and inserting in place thereof the following 2 subsections:-
126 (b)(1) There shall be a board, with duties and powers established by this chapter, which 
127shall govern the commission. The board shall consist of the following members: the secretary of 
128administration and finance, ex officio; the secretary of health and human services, ex officio; 7 
129members to be appointed by the governor pursuant to paragraph (2), 1 of whom shall serve as 
130chair; and 4 members to be appointed by the attorney general. Each appointment after the initial 
131term of appointment shall serve a term of 5 years; provided, however, that a person appointed to 
132fill a vacancy shall serve for not more than the unexpired term. An appointed member of the 
133board shall be eligible for reappointment; provided, however, that no appointed member shall 
134concurrently hold full or part-time employment in the executive branch. The board shall annually 
135elect 1 of its members to serve as vice-chairperson. Each member of the board shall be a resident 
136of the commonwealth. A member of the board serving ex officio may appoint a designee under 
137section 6A of chapter 30; provided further, however, that designee members shall not serve as 
138chair or vice-chair.
139 (2) The person appointed by the governor to serve as chair shall have demonstrated 
140expertise in health care administration, finance and management at a senior level. The second 
141person appointed by the governor shall be a registered nurse with expertise in the delivery of care 
142and development and utilization of innovative treatments in the practice of patient care. The third 
143person appointed by the governor shall have demonstrated expertise in health plan administration  9 of 119
144and finance. The fourth person appointed by the governor shall have demonstrated expertise in 
145representing the health care workforce as a leader in a labor organization. The fifth person 
146appointed by the governor shall have demonstrated expertise in development and pricing for 
147pharmaceuticals, biotechnology or medical devices. The sixth person appointed by the governor 
148shall be a primary care physician. The seventh person appointed by the governor shall have 
149demonstrated expertise as a purchaser of health insurance representing business management or 
150health benefits administration. The first person appointed by the attorney general shall have 
151demonstrated expertise in hospitals or hospital health systems administration, finance or 
152management. The second person appointed by the attorney general shall have demonstrated 
153expertise in health care consumer advocacy. The third person appointed by the attorney general 
154shall have expertise in behavioral health, substance use disorder, mental health services and 
155mental health reimbursement systems. The fourth person appointed by the attorney general shall 
156be a health economist.
157 (c) Seven members of the board shall constitute a quorum, and the affirmative vote of 6 
158members of the board shall be necessary and sufficient for any action taken by the board. No 
159vacancy in the membership of the board shall impair the right of a quorum to exercise all the 
160rights and duties of the commission. The appointed members of the board shall receive a stipend 
161in an amount not more than 10 per cent of the salary of the secretary of administration and 
162finance under section 4 of chapter 7; provided, however, that the chairperson shall receive a 
163stipend in an amount not more than 12 per cent of the salary of the secretary; and provided 
164further, that ex officio members and their designees shall not receive a stipend for their service as 
165board members. Appointed members of the board shall be special state employees subject to 
166chapter 268A. An appointed member of the board shall not be employed by, a consultant to, a  10 of 119
167member of the board of directors of or otherwise be a representative of a health care entity, 
168pharmaceutical manufacturer or pharmacy benefit manager while serving on the board.
169 SECTION 18. Said chapter 6D is hereby further amended by inserting after section 3 the 
170following section:- 
171 Section 3A. (a) There shall be within the commission an office for pharmaceutical policy 
172and analysis. The office shall: (i) issue reports including, but not limited to, an annual report 
173pursuant to subsection (b) and analyses of: (A) pharmaceutical spending in the commonwealth; 
174the affordability of and access to pharmaceutical drugs; (B) the potential innovation of high 
175value drugs and orphan drugs; and (C) the impacts of these issues on racially and ethnically 
176diverse populations and individuals with disabilities; (ii) analyze pharmaceutical data collected 
177by agencies of the commonwealth including, but not limited to, pharmaceutical data collected by 
178the center pursuant to sections 8 to 10, inclusive, of chapter 12C and pharmaceutical data 
179available through public and proprietary sources; provided, however, that the commission may 
180solicit additional data and information directly from manufacturers, pharmacy benefit managers 
181and payers to the extent necessary to perform the duties set forth in this section, including, but 
182not limited to, conducting an annual survey of payers on pharmaceutical access and plan design; 
183provided, however, that confidential data shall not be a public record and shall be exempt from 
184disclosure pursuant to clause Twenty-sixth of section 7 of chapter 4 and section 10 of chapter 66; 
185(iii) assess the value and pricing of pharmaceutical drugs used in the commonwealth including, 
186but not limited to, reviewing disclosures submitted pursuant to section 8A; and (iv) advise other 
187state agencies and entities including, but not limited to, the executive office of health and human 
188services, the office of Medicaid, the division of insurance, the group insurance commission, the 
189commonwealth health insurance connector authority, the department of corrections, the  11 of 119
190Massachusetts Life Sciences Center and the joint committee on health care financing on actions, 
191including any proposed legislation, that may improve the value and pricing of pharmaceutical 
192drugs in the commonwealth.
193 (b) The commission shall compile an annual report concerning trends and underlying 
194factors for pharmaceutical drug spending including, but not limited to, analysis of: (i) prices and 
195utilization; (ii) drugs or categories of drugs with the highest impact on spending; (iii) trends in 
196patient out-of-pocket spending; and (iv) any recommendations for strategies to reduce 
197pharmaceutical spending growth, promote affordability and enhance pharmaceutical access. The 
198report shall be based on: (A) the commission’s analysis of information provided at the annual 
199health care cost trends hearings by providers, provider organizations and insurers; (B) data 
200collected by the center for health information and analysis under sections 8 to10, inclusive, of 
201chapter 12C; and (C) any other information the commission considers necessary to fulfill its 
202duties under this section, as further defined in regulations promulgated by the commission. 
203Annually, not later than December 31, the commission shall submit the report to the chairs of the 
204house and senate committees on ways and means and the chairs of the joint committee on health 
205care financing and shall publish and make the report available to the public.
206 SECTION 19. Said chapter 6D is hereby further amended by striking out section 4, as 
207appearing in the 2022 Official Edition, and inserting in place thereof the following section:- 
208 Section 4. There shall be an advisory council to the commission. The council shall advise 
209on the overall operation and policy of the commission. The commission shall convene the 
210council quarterly or more frequently as requested by the commission. Members of the board of 
211the health policy commission shall convene and consult with advisory council members on  12 of 119
212issues brought before the commission and shall present the views of advisory council members 
213in board meetings. The council shall be appointed by the executive director and reflect a broad 
214distribution of diverse perspectives on the health care system, including, but not limited to, 
215health care professionals, educational institutions, consumer representatives, purchasers of health 
216insurance representing business management or health benefits administration, medical device 
217manufacturers, representatives of the biotechnology industry, pharmaceutical manufacturers, 
218providers, provider organizations, hospitals, community health centers, labor organizations and 
219public and private payers.
220 SECTION 20. Section 5 of said chapter 6D, as so appearing, is hereby amended by 
221inserting after the word “growth”, in line 3, the following words:- and affordability.
222 SECTION 21. Said section 5 of said chapter 6D, as so appearing, is hereby further 
223amended by striking out, in line 10, the words “and (vii)” and inserting in place thereof the 
224following words:- ; (vii) monitor pharmaceutical spending and pricing and patient access to 
225pharmaceuticals; and (viii).
226 SECTION 22. The 	first paragraph of section 6 of said chapter 6D, as so appearing, is 
227hereby amended by adding the following sentence:-
228 Each pharmaceutical manufacturing company and pharmacy benefit manager shall pay to 
229the commonwealth an amount for the estimated expenses of the center and for the other purposes 
230described in this chapter.
231 SECTION 23. Said section 6 of said chapter 6D, as so appearing, is hereby further 
232amended by striking out, in lines 5 and 36, the figure “33”, each time it appears, and inserting in 
233place thereof, in each instance, the following figure:- 25. 13 of 119
234 SECTION 24. Said section 6 of said chapter 6D, as so appearing, is hereby further 
235amended by adding the following 3 paragraphs:-
236 To the maximum extent permissible under federal law, provided that such assessment 
237will not result in any reduction of federal financial participation in Medicaid, the assessed 
238amount for pharmaceutical manufacturing companies shall be not less than 25 per cent of the 
239amount appropriated by the general court for the expenses of the commission less amounts 
240collected from: (i) filing fees; (ii) fees and charges generated by the commission's publication or 
241dissemination of reports and information; and (iii) federal matching revenues received for said 
242expenses or received retroactively for expenses of predecessor agencies. Pharmaceutical 
243manufacturing companies shall pay such assessed amount multiplied by the ratio of the 
244pharmaceutical manufacturing company’s gross sales of outpatient prescription drugs dispensed 
245in the commonwealth or similar measure determined by the commission consistent with 
246applicable federal requirements. 
247 To fund the operations of the commonwealth’s licensure of pharmacy benefit managers 
248and to the maximum extent permissible under federal law; provided, however, that such 
249assessment will not result in any reduction of federal financial participation in Medicaid, the 
250assessed amount for pharmacy benefit managers shall be not less than 25 per cent of the amount 
251appropriated by the general court for the expenses of the commission less amounts collected 
252from: (i) filing fees; (ii) fees and charges generated by the commission's publication or 
253dissemination of reports and information; and (iii) federal matching revenues received for said 
254expenses or received retroactively for expenses of predecessor agencies. Pharmacy benefit 
255managers shall pay such assessed amount multiplied by the ratio of the pharmacy benefit 
256manager’s gross revenue related to outpatient prescription drugs dispensed in the commonwealth  14 of 119
257or similar measure determined by the commission consistent with applicable federal 
258requirements. In no event shall this assessment, when combined with an assessment of pharmacy 
259benefit managers pursuant to section 7 of chapter 12C and a pharmacy benefit manager licensing 
260fee pursuant to section 2 of chapter 176Y, exceed the commonwealth’s estimated expense in 
261operating the pharmacy benefit manager licensure program.  
262 Each pharmaceutical manufacturing company and each pharmacy benefit manager shall 
263make a preliminary payment to the commission annually on October 1 in an amount equal to 1/2 
264of the initial year’s total assessment and, for subsequent years, in an amount equal to 1/2 of the 
265previous year's total assessment. Thereafter, each pharmaceutical manufacturing company and 
266each pharmacy benefit manager shall pay, within 30 days of receiving notice from the 
267commission, the balance of the total assessment for the current year as determined by the 
268commission.
269 SECTION 25. Section 7 of said chapter 6D, as so appearing, is hereby amended by 
270striking out, in line 35, the words “and (vi)” and inserting in place thereof the following words:- 
271(vi) advance health equity; and (vii). 
272 SECTION 26. Said chapter 6D is hereby further amended by striking out section 8, as so 
273appearing, and inserting in place thereof the following section:- 
274 Section 8. (a) Not later than October 1 of every year, the commission shall hold public 
275hearings based on the report submitted by the center pursuant to section 16 of chapter 12C 
276comparing: (i) the average of the annual growth in total health care expenditures during each 
277year of the most recently concluded benchmark cycle to the health care cost growth benchmark 
278for that benchmark cycle; and (ii) the growth in the affordability index pursuant to said section  15 of 119
27916 of said chapter 12C to the affordability benchmark. At said hearings, the commission shall 
280examine the costs, prices and cost trends of health care providers, provider organizations, private 
281and public health care payers, pharmaceutical manufacturing companies and pharmacy benefit 
282managers and any relevant impact of private equity firms, real estate investment trusts and 
283management services organizations on such costs, prices and cost trends, with particular 
284attention to factors that contribute to cost growth within the commonwealth's health care system 
285and trends in annual behavioral health expenditures.
286 (b) The attorney general may intervene in such hearings.
287 (c) Public notice of any hearing shall be provided not less than 60 days in advance.
288 (d) The commission shall identify as witnesses for the public hearing a representative 
289sample of providers, provider organizations, payers, private equity firms, real estate investment 
290trusts, management services organizations, pharmaceutical manufacturing companies, pharmacy 
291benefit managers and others, including: (i) not less than 3 academic medical centers, including 
292the 2 acute hospitals with the highest level of net patient service revenue; (ii) not less than 3 
293disproportionate share hospitals, including the 2 hospitals whose largest per cent of gross patient 
294service revenue is attributable to Title XVIII and XIX of the Social Security Act or other 
295governmental payers; (iii) community hospitals from not less than l 3 separate regions of the 
296commonwealth; (iv) freestanding ambulatory surgical centers from not less than 3 separate 
297regions of the commonwealth; (v) community health centers from at not less than 3 separate 
298regions of the commonwealth; (vi) the 5 commercial carriers with the highest enrollments in the 
299commonwealth; (vii) any managed care organization that provides health benefits under Title 
300XIX of the Social Security Act ; (viii) the group insurance commission; (ix) not less than 3  16 of 119
301municipalities that have adopted chapter 32B; (x) not less than 4 provider organizations which 
302shall be from diverse geographic regions of the commonwealth, not less than 2 of which shall be 
303certified as accountable care organizations and 1 of which shall be certified as a model ACO; (xi) 
304at least 1 private equity firms, real estate investment trust or management services organization 
305associated with a provider or provider organization; (xii) the assistant secretary for MassHealth; 
306(xiii) not less than 3 representatives of pharmaceutical manufacturing companies doing business 
307in the commonwealth or trade groups thereof; (xiv) 1 	pharmacy benefit manager or trade groups 
308thereof; and (xv) any witness identified by the attorney general or the center. 
309 (e) Witnesses shall provide testimony under oath and subject to examination and cross 
310examination by the commission, the executive director of the center and the attorney general at 
311the public hearing in a manner and form to be determined by the commission, including, but not 
312limited to: (i) in the case of providers and provider organizations, testimony concerning payment 
313systems, care delivery models, payer mix, cost structures, administrative and labor costs, capital 
314and technology cost, adequacy of public payer reimbursement levels, reserve levels, utilization 
315trends, relative price, quality improvement and care-coordination strategies, investments in 
316health information technology, the relation of private payer reimbursement levels to public payer 
317reimbursements for similar services, efforts to improve the efficiency of the delivery system, 
318efforts to reduce the inappropriate or duplicative use of technology and the impact of price 
319transparency on prices; (ii) in the case of private and public payers, testimony concerning factors 
320underlying premium cost and rate increases, the relation of reserves to premium costs, efforts by 
321the payer to reduce the use of fee-for-service payment mechanisms, the payer's efforts to develop 
322benefit design, network design and payment policies that enhance product affordability and 
323encourage efficient use of health resources and technology including utilization of alternative  17 of 119
324payment methodologies, efforts by the payer to increase consumer access to health care 
325information, efforts by the payer to promote the standardization of administrative practices, the 
326impact of price transparency on prices and any other matters as determined by the commission; 
327(iii) in the case of the assistant secretary for MassHealth, testimony concerning the structure, 
328benefits, eligibility, caseload and financing of MassHealth and other Medicaid programs 
329administered by the office of Medicaid or in partnership with other state and federal agencies and 
330the agency’s activities to align or redesign said programs in order to encourage the development 
331of more integrated and efficient health care delivery systems; (iv) in the case of private equity 
332firms, real estate investment trusts or management services organization, testimony concerning 
333changes to patient access to health care services or facilities, health outcomes, prices charged to 
334insurers and patients, staffing levels, clinical workflow, financial stability and ownership 
335structure as the result of an acquisition of a provider or provider organization, the amount of debt 
336and equity leveraged in an acquisition of a provider or provider organization, additional debt 
337taken on by a provider or provider organization after an acquisition, dividends paid out to 
338investors, changes to real estate ownership and any leaseback agreements and management of 
339clinical assets and any other matters as determined by the commission; and (v) in the case of 
340pharmacy benefit managers and pharmaceutical manufacturing companies, testimony concerning 
341factors underlying prescription drug costs and price changes including, but not limited to, the 
342initial prices of drugs coming to market and subsequent price changes, changes in industry profit 
343levels, marketing expenses, reverse payment patent settlements, impacts of manufacturer rebates, 
344discounts and other price concessions on net pricing, 	availability of alternative drugs or 
345treatments, corporate ownership organizational structure and any other matters as determined by 
346the commission. The commission shall solicit testimony from a payer which has been identified  18 of 119
347by the center's annual report under subsection (a) of section 16 of chapter 12C as: (A) paying 
348providers more than 10 per cent above or more than 10 per cent below the average relative price; 
349or (B) entering into alternative payment contracts that vary by more than 10 per cent. A payer 
350identified by the center's report shall explain the extent of price variation between the payer's 
351participating providers and describe any efforts to reduce such price variation.
352 (f) If the center's annual report pursuant to subsection (a) of section 16 of chapter 12C 
353finds that the average of the annual percentage changes in total health care expenditures during a 
354benchmark cycle exceeded the health care cost growth benchmark for that benchmark cycle or 
355the percentage change in the affordability index exceeded the affordability benchmark, the 
356commission may identify additional witnesses for the public hearing. Witnesses shall provide 
357testimony subject to examination and cross examination by the commission, the executive 
358director of the center and attorney general at the public hearing in a manner and form to be 
359determined by the commission, including, but not limited to: (i) testimony concerning 
360unanticipated events that may have impacted the total health care cost expenditures and 
361affordability, including, but not limited to, a public health crisis such as an outbreak of a disease, 
362a public safety event or a natural disaster; (ii) testimony concerning trends in patient acuity, 
363complexity or utilization of services; (iii) testimony concerning trends in input cost structures, 
364including, but not limited to, the introduction of new pharmaceuticals, medical devices and other 
365health technologies; (iv) testimony concerning the cost of providing certain specialty services, 
366including, but not limited to, the provision of health care to children, cancer-related health care 
367and medical education; (v) testimony related to unanticipated administrative costs for carriers, 
368including, but not limited to, costs related to information technology, administrative 
369simplification efforts, labor costs and transparency efforts; (vi) testimony related to costs due the  19 of 119
370implementation of state or federal legislation or government regulation; (vii) testimony related to 
371premiums by market segment and community, plan and benefit design and cost sharing, 
372including deductibles and co-pays; and (viii) any other factors that may have led to excessive 
373health care cost growth.
374 (g) The commission shall annually compile a report for the most recently concluded 
375benchmark cycle concerning spending trends, including primary care and behavioral health 
376expenditures, affordability and the underlying factors influencing said spending trends. The 
377report shall be based on the commission’s analysis of information provided at the hearings by 
378witnesses, providers, provider organizations, payers, private equity firms, real estate investment 
379trusts, management services organizations, pharmaceutical manufacturing companies and 
380pharmacy benefit managers, registration data collected pursuant to section 11, data collected or 
381analyzed by the center pursuant to sections 8 to 10A, inclusive, of chapter 12C and any other 
382available information that the commission considers necessary to fulfill its duties under this 
383section, as further defined in regulations promulgated by the commission. To the extent 
384practicable, the report shall not contain any data that is likely to compromise the financial, 
385competitive or proprietary nature of the information. The report shall be submitted to the chairs 
386of the house and senate committees on ways and means and the chairs of the joint committee on 
387health care financing and shall be published and made available to the public annually, not later 
388than December 31, of each year. The report shall include recommendations for strategies to 
389increase the efficiency of the health care system and promote affordability for individuals and 
390families and analysis of specific spending trends that 	may impede the commonwealth’s ability to 
391meet the health care cost growth benchmark, together with any drafts of legislation language 
392necessary to implement said recommendations. 20 of 119
393 SECTION 27. Said chapter 6D is hereby further amended by striking out sections 9 and 
39410, as so appearing, and inserting in place thereof the 	following 3 sections:- 
395 Section 9. (a) Not later than April 15 of every year, the board shall establish the health 
396care cost growth benchmark for a benchmark cycle consisting of the 2 calendar years beginning 
397after the year in which the April 15 date occurs. 
398 (b) The health care cost growth benchmark shall be equal to the average of the growth 
399rate of potential gross state product established under section 7H½ of chapter 29 for each of the 2 
400calendar years that comprise the benchmark cycle. The commission shall establish procedures to 
401prominently publish the health care cost growth benchmark on the commission’s website.
402 (c) For all benchmark cycles through the cycle containing the calendar years 2039 and 
4032040, if the commission determines that an adjustment in the health care cost growth benchmark 
404is reasonably warranted, having first considered any testimony at a public hearing as required 
405under subsection (d), the board of the commission may recommend a modification of the health 
406care cost growth benchmark, in any amount as determined by the commission. The board shall 
407submit notice of its recommendation for any modification to the joint committee on health care 
408financing. Within 30 days of such filing, the joint committee may hold a public hearing on the 
409board's proposed modification to the health care cost growth benchmark. Within 30 days of the 
410public hearing, the joint committee may report its findings and proposed legislation, including its 
411recommendation on whether to affirm or reject the boards’ recommendation, to the general court 
412and provide a copy of its findings and proposed legislation to the board.
413 (d) Prior to making any recommended modification to the health care cost growth 
414benchmark under subsection (c), the board shall hold a public hearing on any such recommended  21 of 119
415modification. The public hearing shall be based on the report submitted by the center pursuant to 
416section 16 of chapter 12C comparing the average of the annual growth in total health care 
417expenditures during each year of the most recently concluded benchmark cycle to the health care 
418cost growth benchmark, any other data provided by the center and such other pertinent 
419information or data as may be available to the board. The hearing shall examine the costs, prices 
420and cost trends of health care provider, provider organization and private and public health care 
421payer and any relevant impact of private equity firms, real estate investment trusts, management 
422services organizations, pharmaceutical manufacturing companies and pharmacy benefit 
423managers on such costs, prices and cost trends, with particular attention to factors that contribute 
424to cost growth within the commonwealth’s health care system and whether, based on the 
425testimony, information and data presented at the hearing, a modification in the health care cost 
426growth benchmark is appropriate. The commission shall provide public notice of such hearing 
427not less than 45 days prior to the date of the hearing, including notice to the joint committee on 
428health care financing. The joint committee on health care financing may participate in the 
429hearing. The commission shall identify as witnesses for the public hearing a representative 
430sample of providers, provider organizations, payers, private equity firms, real estate investment 
431trusts, management services organizations, pharmaceutical manufacturing companies, pharmacy 
432benefit managers and such other interested parties as the commission may determine. Any other 
433interested parties may testify at the hearing. 
434 (e) Any recommendation of the commission to modify the health care cost growth 
435benchmark under subsection (c) of this section shall be approved by a two-thirds vote of the 
436board.  22 of 119
437 Section 9A. Not later than April 15 of every year, the board shall establish a health care 
438affordability benchmark for the following calendar year. The commission shall establish 
439procedures to prominently publish the annual affordability benchmark on the commission's 
440website.
441 Section 10. (a) For the purpose of this section, “Health care entity” shall mean any health 
442care entity identified by the center pursuant to section 18 of chapter 12C.
443 (b) The commission shall provide notice to a health care entity that the commission may 
444analyze the health care spending performance of such health care entity and that such health care 
445entity shall perform certain actions as provided in subsection (c); provided, however, that at the 
446discretion of the commission, the commission may publicly identify the identities and 
447performance results of such health care entity.
448 (c) The commission may require a performance improvement plan to be filed with the 
449commission for a health care entity that is identified by the center under section 18 of chapter 
45012C.
451 (d) In addition to the notice provided under subsection (b), the commission shall provide 
452written notice to a health care entity that it determines must file a performance improvement 
453plan. Within 45 days of receipt of such written notice, the health care entity shall either:
454 (1) file a performance improvement plan with the commission; or
455 (2) file an application with the commission to waive or extend the requirement to file a 
456performance improvement plan. 23 of 119
457 (e) The health care entity may file documentation or supporting evidence with the 
458commission to support the health care entity’s application to waive or extend the requirement to 
459file a performance improvement plan. The commission shall require the health care entity to 
460submit any other relevant information it deems necessary in considering the waiver or extension 
461application; provided, however, that such information shall be made public at the discretion of 
462the commission.
463 (f) The commission may waive or delay the requirement for a health care entity to file a 
464performance improvement plan in response to a waiver or extension request filed under 
465subsection (d) in light of all information received from the health care entity, based on a 
466consideration of the following factors:
467 (1) the spending, price and utilization trends of the health care entity over time, 
468independently and as compared to similar entities, and any demonstrated improvement to reduce 
469spending or total medical expenses;
470 (2) any ongoing strategies or investments that the health care entity is implementing to 
471improve future long-term efficiency and reduce spending growth;
472 (3) whether the factors that led to increased spending for the health care entity can 
473reasonably be considered to be unanticipated and outside of the control of the entity. Such factors 
474may include, but shall not be limited to, age and other health status adjusted factors and other 
475cost inputs such as pharmaceutical expenses, medical device expenses and labor costs;
476 (4) the overall financial condition of the health care entity;  24 of 119
477 (5) a significant difference between the growth rate of potential gross state product and 
478the growth rate of actual gross state product, as determined under section 7H½ of chapter 29; and
479 (6) any other factors the commission considers relevant.
480 (g) If the commission declines to waive or extend the requirement for the health care 
481entity to file a performance improvement plan, the commission shall provide written notice to the 
482health care entity that its application for a waiver or extension was denied and the health care 
483entity shall file a performance improvement plan.
484 (h) A health care entity shall file a performance improvement plan: (A) within 45 days of 
485receipt of a notice under subsection (d); (B) if the health care entity has requested a waiver or 
486extension, within 45 days of receipt of a notice that such waiver or extension has been denied; or 
487(C) if the health care entity is granted an extension, on the date given on such extension. The 
488performance improvement plan shall identify the causes of the entity's excessive spending, and 
489shall include, but not be limited to, specific strategies, adjustments and action steps the entity 
490proposes to implement to improve spending performance. The proposed performance 
491improvement plan shall include specific identifiable and measurable expected outcomes and a 
492timetable for implementation. The timetable for a performance improvement plan shall not 
493exceed 18 months.
494 (i) The commission shall approve any performance improvement plan that it determines 
495is reasonably likely to address the underlying cause of the health care entity’s excessive spending 
496and has a reasonable expectation for successful implementation. 25 of 119
497 (j) If the board determines that the performance improvement plan is unacceptable or 
498incomplete, the commission may provide consultation on the criteria that have not been met and 
499may allow an additional time period of not more than 30 calendar days, for resubmission.
500 (k) Upon approval of the proposed performance improvement plan, the commission shall 
501notify the health care entity to begin implementation of the performance improvement plan. 
502Public notice shall be provided by the commission on its website, identifying that the health care 
503entity is implementing a performance improvement plan. Health care entities implementing an 
504approved performance improvement plan shall be subject to additional reporting requirements 
505and compliance monitoring, as determined by the commission. The commission shall assist the 
506health care entity with the successful implementation of the performance improvement plan.
507 (l) Health care entities subject to a performance improvement plan shall, in good faith, 
508work to implement such plan and may file amendments to the performance improvement plan at 
509any point during the implementation of the performance improvement plan, subject to approval 
510of the commission.
511 (m) At the conclusion of the timetable established in the performance improvement plan, 
512the health care entity shall report to the commission regarding the outcome of the performance 
513improvement plan. If the commission finds that the performance improvement plan was 
514unsuccessful, the commission shall either: (i) extend the implementation timetable of the existing 
515performance improvement plan; (ii) approve amendments to the performance improvement plan 
516as proposed by the health care entity; (iii) require the health care entity to submit a new 
517performance improvement plan under subsection (c), including requiring specific elements for  26 of 119
518approval; or (iv) waive or delay the requirement to file any additional performance improvement 
519plans.
520 (n) Upon the successful completion of the performance improvement plan, the identity of 
521the health care entity shall be removed from the list of entities currently implementing a 
522performance improvement plan on the commission’s website.
523 (o) The commission may submit a recommendation for proposed legislation to the joint 
524committee on health care financing if the commission determines that further legislative 
525authority is needed to achieve the commonwealth’s health care quality and spending 
526sustainability objectives, assist health care entities with the implementation of performance 
527improvement plans or otherwise ensure compliance with the provisions of this section.
528 (p)(1) If the commission determines that a health care entity has: (i) willfully neglected to 
529file a performance improvement plan with the commission within 45 days as required under 
530subsection (d); (ii) failed to file an acceptable performance improvement plan in good faith with 
531the commission; (iii) failed to implement the performance improvement plan in good faith; or 
532(iv) knowingly failed to provide or falsified information required by this section to the 
533commission, the commission may: (A) assess a civil penalty to the health care entity of not more 
534than $500,000 for a first violation, not more than $750,000 for a second violation and not more 
535than $1,000,000 for a third or subsequent violation; provided, however, that a civil penalty 
536assessed pursuant to one of the above clauses shall be a first offense if a previously assessed 
537penalty was assessed pursuant to a different clause; (B) stay consideration of any material change 
538notice submitted under section 13 of this chapter by the health care entity or any affiliates until 
539the commission determines that the health care entity is in compliance with this section; and (C)  27 of 119
540notify the department of public health that the health care entity, if applying for a notice of 
541determination of need, is not in compliance with this section. A civil penalty assessed under this 
542subsection shall be deposited into the Healthcare Payment Reform Fund established under 
543section 100 of chapter 194 of the acts of 2011. Except as otherwise expressly authorized under 
544this section, the commission shall seek to promote compliance with this section and shall only 
545impose a civil penalty as a last resort.
546 (2) In lieu of requiring a performance improvement plan pursuant to this section, the 
547commission may assess a civil penalty on a health care entity identified by the center pursuant to 
548section 18 of chapter 12C if the commission determines that a performance improvement plan is 
549not an appropriate remedial measure. The civil penalty may amount to not more than the amount 
550of spending attributable to the health care entity that is in excess of the health care cost growth 
551benchmark and shall be deposited into the Healthcare Payment Reform Fund established under 
552section 100 of chapter 194 of the acts of 2011. Prior to assessing the civil penalty, the 
553commission shall provide the health care entity with written notice of its intent to assess the 
554penalty; provided, however, that the commission shall provide the health care entity not less than 
55510 days to respond to said written notice with a written request for a hearing; provided further, 
556that, if the health care entity requests a hearing, the commission shall hold the hearing within 30 
557days of the commission’s receipt of the request; and provided further, that if the health care 
558entity does not request a hearing, the commission shall provide the health care entity with not 
559less than 30 days to respond in writing to said written notice.
560 (q) The commission shall promulgate regulations necessary to implement this section; 
561provided, however, that notice of any proposed regulations shall be filed with the joint  28 of 119
562committee on state administration and regulatory oversight and the joint committee on health 
563care financing not less than180 days before adoption. 
564 SECTION 28. Section 11 of said chapter 6D, as so appearing, is hereby amended by 
565striking out, in line 3, the words “2 years” and inserting in place thereof the following words:- 1 
566year.
567 SECTION 29. Said section 11 of said chapter 6D, as so appearing, is hereby further 
568amended by striking out subsection (b) and inserting in place thereof the following subsection:- 
569 (b) The commission shall require that all provider organizations report information 
570detailed in section 9 of chapter 12C. The commission may specify additional data elements in a 
571given reporting year to support the development of the state health plan or the focused 
572assessments defined in section 22 of chapter 6D.
573 SECTION 30. Said section 11 of said chapter 6D, as so appearing, is hereby further 
574amended by striking out subsection (d) and inserting in place thereof the following subsection:-
575 (d) The commission may enter into interagency agreements with the center and other 
576state agencies to effectuate the goals of this section.
577 SECTION 31. Said chapter 6D is hereby further amended by striking out sections 12 and 
57813, as so appearing, and inserting in place thereof the 	following 2 sections:- 
579 Section 12. (a) The commission shall ensure the timely reporting of information required 
580under section 11. The commission shall notify provider organizations of any applicable reporting 
581deadlines; provided, that the commission shall notify, in writing, a provider organization that has 
582failed to meet a reporting deadline and that failure to respond within 2 weeks of the receipt of the  29 of 119
583notice may result in penalties. The commission may assess a penalty against a provider 
584organization that fails, without just cause, to provide the requested information within 2 weeks 
585following receipt of the written notice required under this subsection of up to $10,000 per week 
586for each week of delay after the 2-week period following provider organization's receipt of the 
587written notice; provided, however, that the maximum annual penalty against a provider 
588organization under this section shall be $500,000 per registration cycle. Amounts collected under 
589this section shall be deposited in the Healthcare Payment Reform Fund established under section 
590100 of chapter 194 of the Acts of 2011.  
591 (b) Notwithstanding any general or special law to the contrary, any material change 
592notice submitted under section 13 and any determination of need application submitted under 
593sections 25B to 25G, inclusive, of chapter 111 by a provider organization that has failed to 
594provide required information pursuant to section 11 and section 9 of chapter 12C shall be 
595incomplete until such time as the provider organization has provided such required information. 
596 (c) Nothing in this chapter shall require a provider organization which represents 
597providers who collectively receive, less than $25,000,000 in annual net patient service revenue to 
598be registered if such provider or provider organization is not a risk-bearing provider organization 
599or is not owned or controlled, whether fully or partially, directly or indirectly, by a private equity 
600firm.
601 Section 13. (a)(1) Every provider or provider organization shall, before making any 
602material change to its operations or governance structure, submit notice to the commission, the 
603center and the attorney general of such change not less than 60 days before the date of the 
604proposed change, provided, however, that material changes shall include, but not be limited to:  30 of 119
605(i) significant expansions in a provider or provider organization’s capacity; (ii) a corporate 
606merger, acquisition or affiliation of a provider or provider organization and a carrier; (iii) 
607mergers or acquisitions of hospitals or hospital systems; (iv) acquisition of insolvent provider 
608organizations; (v) significant new for-profit investment in, acquisitions of the assets of or 
609ownership or direct or indirect control of a provider or provider organization by for-profit 
610entities, including, but not 	limited to, private equity firms and management services 
611organizations; (vi) substantial acquisition or sale of assets for an ownership share or for the 
612purposes of a lease-back arrangement; (vii) conversion of a provider or provider organization 
613from a non-profit entity to a for-profit entity; and (viii) mergers or acquisitions of provider 
614organizations which will result in a provider organization having a dominant market share in a 
615given service or region.
616 Within 30 days of receipt of a completed notice filed under the commission’s regulations, 
617the commission shall conduct a preliminary review to determine whether the material change is 
618likely to result in a significant impact on the commonwealth’s ability to meet the health care cost 
619growth benchmark established in section 9, or on the competitive market. If the commission 
620finds that the material change is likely to have a significant impact on the commonwealth’s 
621ability to meet the health care cost growth benchmark, or on the competitive market, the 
622commission may conduct a cost and market impact review under this section.
623 (2) If the commission determines that a proposed material change is likely to have a 
624significant negative impact on health care consumers in the commonwealth, including through 
625significantly increased costs, significantly reduced quality, or significantly impaired access to 
626health care services, including for at-risk, underserved and government payer patient 
627populations, the commission may recommend modifications to the proposed material change to  31 of 119
628mitigate such impacts. Notwithstanding any general or special law to the contrary, failure to 
629modify the proposed material change to substantially address such impacts identified by the 
630commission shall constitute an unfair business practice under chapter 93A subject to challenge 
631pursuant to section 4 of said chapter 93A but not pursuant to sections 9 or 11 of said chapter 
63293A. The commission shall notify the office of the attorney general of any provider or provider 
633organization’s failure to modify the proposed material change to substantially address such 
634impacts. 
635 (b) In addition to the grounds for a cost and market impact review set forth in subsection 
636(a), if the commission finds, based on the center’s benchmark cycle report under section 16 of 
637chapter 12C, that the average of the annual percentage changes in total health care expenditures 
638during each year of the benchmark cycle exceeded the health care cost growth benchmark for 
639that benchmark cycle, the commission may conduct a cost and market impact review of any 
640provider organization identified by the center under section 18 of said chapter 12C.
641 (c)(1) The commission shall initiate a cost and market impact review by sending the 
642provider or provider organization notice of a cost and market impact review, which shall explain 
643the basis for the review and the particular factors that the commission seeks to examine through 
644the review. The provider or provider organization shall submit to the commission, within 21 days 
645of the commission’s notice, a written response to the notice, including, but not limited to, any 
646information or documents sought by the commission that are described in the commission’s 
647notice. The commission may require that any provider, provider organization, payer, investor or 
648other party associated with a given transaction submit documents and information in connection 
649with a notice of material change or a cost and market impact review under this section. The 
650commission may also require, for a period of 5 years following the completion of a material  32 of 119
651change, that any provider or provider organization submit data and information to assess the 
652post-transaction impacts of a material change and compliance with any commitments or 
653conditions agreed to by the parties. The commission shall keep confidential all nonpublic 
654information and documents obtained under this section and shall not disclose the information or 
655documents to any person without the consent of the provider or payer that produced the 
656information or documents, except in a preliminary report or final report under this section if the 
657commission believes that such disclosure should be made in the public interest after taking into 
658account any privacy, trade secret or anti-competitive considerations. The confidential 
659information and documents shall not be public records and shall be exempt from disclosure 
660under clause Twenty-sixth of section 7 of chapter 4 or section 10 of chapter 66.
661 (2) For any material change involving significant new for-profit investment in, 
662acquisitions of the assets of or ownership or direct or indirect control of a provider or provider 
663organization by a for-profit entity, the for-profit entity, and the parent company or person or 
664persons controlling the for-profit entity, if any, will be required to submit, at a minimum, the 
665following information to complete the notice: (i) information regarding the capital structure, 
666general financial condition, ownership and management of the for-profit entity and any person 
667controlling the for-profit entity; (ii) the identity and relationship of every member of the for-
668profit entity; (iii) fully audited financial information for the preceding 5 fiscal years or for such 
669lesser period as the for-profit entity and any predecessors thereof shall have been in existence; 
670(iv) any plans or proposals to liquidate such provider or provider organization, to sell its assets or 
671merge or consolidate it with any person, or to make any other material change in its business or 
672corporate structure or management; (v) fully audited financial information of all health care 
673entities acquired by the for-profit entity, the parent company and person or persons controlling  33 of 119
674the for-profit entity, for the preceding 5 fiscal years or for such lesser period as the for-profit 
675entity and any predecessors thereof shall have been in existence as well as other financial 
676information the commission deems relevant, including, but not limited to, bankruptcy filings, 
677sales of non-clinical assets and dividend recapitalizations; (vi) operational information regarding 
678health care entities acquired by the acquiring party or person or persons controlling the acquiring 
679party for the preceding 10 fiscal years or for such lesser period as such acquiring party and any 
680predecessors thereof shall have been in existence, including, but not limited to, reduction or 
681closure of health care services; and (vii) such additional information as the commission may 
682deem necessary or appropriate for the protection of essential health services or to evaluate the 
683material change notice.
684 (d) A cost and market impact review may examine factors relating to the provider or 
685provider organization’s business and its relative market position, including, but not limited to: (i) 
686the provider or provider organization’s size and market share within its primary service areas by 
687major service category and within its dispersed service areas; (ii) the provider or provider 
688organization’s prices for services, including its relative price compared to other providers for the 
689same services in the same market; (iii) the provider or provider organization’s health status 
690adjusted total medical expense, including its health status adjusted total medical expense 
691compared to similar providers; (iv) the quality of the services provided by the provider or 
692provider organization, including patient experience; (v) provider cost and cost trends in 
693comparison to total health care expenditures statewide; (vi) the availability and accessibility of 
694services similar to those provided, or proposed to be provided, through the provider or provider 
695organization within its primary service areas and dispersed service areas; (vii) the provider or 
696provider organization’s impact on competing options 	for the delivery of health care services  34 of 119
697within its primary service areas and dispersed service areas, including, if applicable, the impact 
698on existing service providers of a provider or provider organization’s expansion, affiliation, 
699merger or acquisition, to enter a primary or dispersed service area in which it did not previously 
700operate; (viii) the methods used by the provider or provider organization to attract patient volume 
701and recruit or acquire health care professionals or facilities; (ix) the role of the provider or 
702provider organization in serving at-risk, underserved and government payer patient populations, 
703including individuals with behavioral, substance use disorder and mental health conditions, 
704within its primary service areas and dispersed service areas; (x) the role of the provider or 
705provider organization in providing low margin or negative margin services within its primary 
706service areas and dispersed service areas; (xi) consumer concerns, including, but not limited to, 
707complaints or other allegations that the provider or provider organization has engaged in any 
708unfair method of competition or any unfair or deceptive act or practice; (xii) the cumulative 
709impact of mergers, acquisitions, affiliations or joint ventures on the health care market over a 
710reasonable period of time, as defined by the commission; (xiii) alignment with the state health 
711plan and any focused assessments conducted pursuant to section 22; and (xiv) any other factors 
712that the commission determines to be in the public interest.
713 (e) The commission shall make factual findings and issue a preliminary report on the cost 
714and market impact review. In the report, the commission shall identify any provider or provider 
715organization that meets all of the following: (i) the provider or provider organization has, or 
716likely will have as a result of the proposed material change, a dominant market share for the 
717services it provides; (ii) the provider or provider organization charges, or likely will charge as a 
718result of the proposed material change, prices for services that are materially higher than the 
719median prices charged by all other providers for the same services in the same market; and (iii)  35 of 119
720the provider or provider organization has, or likely will have as a result of the proposed material 
721change, a health status adjusted total medical expense that is materially higher than the median 
722total medical expense of comparable providers in the same area.
723 (f) Within 30 days after issuance of a preliminary report, the provider or provider 
724organization may respond in writing to the findings in the report. The commission shall then 
725issue its final report. The commission shall refer to the attorney general its report on any provider 
726or provider organization that meets all 3 criteria under subsection (e). The commission shall 
727issue its final report on the cost and market impact review within 185 days from the date that the 
728provider or provider organization has submitted a completed notice to the commission under the 
729commission’s regulations; 	provided, however, that the provider or provider organization has 
730certified substantial compliance with the commission’s requests for data and information 
731pursuant to subsection (c) within 21 days of the commission’s notice or by a later date set by 
732mutual agreement of the provider or provider organization and the commission.
733 (g) Nothing in this section shall prohibit a proposed material change under subsection (a); 
734provided, however, that any proposed material change shall not be completed: (i) until not later 
735than 30 days after the commission has issued its final report; or (ii) if the attorney general brings 
736an action as described in paragraph (2) of subsection (a) or subsection (h), while such action is 
737pending and prior to a final judgment being issued by a court of competent jurisdiction, 
738whichever is later.
739 (h) A provider or provider organization that meets the criteria in subsection (e) has 
740engaged, or through a material change will engage, in an unfair method of competition or unfair 
741and deceptive trade practice subject to challenge pursuant to section 4 of chapter 93A, but not  36 of 119
742sections 9 or 11 of said chapter 93A. The attorney general may take action under said chapter 
74393A or any other law to protect consumers in the health care market, including by bringing an 
744action seeking to restrain such violation of said chapter 93A. The commission’s final report may 
745be evidence in any such action brought by the attorney general.
746 (i) Nothing in this section shall limit the authority of the attorney general to protect 
747consumers in the health care market under any other law.
748 (j) The commission shall adopt regulations for conducting cost and market impact 
749reviews and for administering this section. These regulations shall include definitions of material 
750change and non-material change, primary service areas, dispersed service areas, dominant market 
751share, materially higher prices, materially higher health status adjusted total medical expenses 
752and any other terms as necessary to provide market participants with appropriate notice. These 
753regulations may identify filing thresholds in connection with this section; provided, however, 
754that the commission shall determine that multiple mergers, acquisitions or affiliations over time 
755may together meet such thresholds. All regulations promulgated by the commission shall comply 
756with chapter 30A.
757 (k) Nothing in this section shall limit the application of other laws or regulations that may 
758be applicable to a provider or provider organization, including laws and regulations governing 
759insurance.
760 (l) Upon issuance of its final report pursuant to subsection (f), the commission shall 
761provide a copy of said final report to the department of public health. The final report shall be 
762included in the written record and considered by the department of public health during its 
763review of an application for determination of need under section 25C of chapter 111 and  37 of 119
764considered where relevant in connection with licensure or other regulatory actions involving the 
765provider or provider organization. 
766 SECTION 32. Said chapter 6D is hereby further amended by adding the following 2 
767sections:-
768 Section 22. (a)(1) Not less than once every 5 years, the commission shall develop a state 
769health plan in consultation with the executive office of health and human services, the 
770department of public health, the office of Medicaid, the department of mental health, the division 
771of insurance, the executive office of elder affairs, the center for health information and analysis 
772and other state agencies as appropriate.
773 (2) The state health plan shall identify: (i) the current and anticipated needs of the 
774commonwealth for health care services, providers, programs and facilities; (ii) the existing health 
775care resources available to meet those needs; (iii) recommendations for the appropriate supply 
776and distribution of resources, workforce, programs, capacities, technologies and services on a 
777statewide and regional basis; (iv) major barriers preventing communities and residents from 
778accessing needed health care; (v) priorities for addressing those barriers; and (vi) 
779recommendations for any further legislative or other state action to assist the commonwealth in 
780achieving the recommendations identified in the plan. 
781 (3) The state health plan shall be based on data from all available sources, including data 
782collected by the commission, the center for health information and analysis, the executive office 
783of health and human services, the department of public health, the office of Medicaid, the 
784department of mental health, the division of insurance, the executive office of elder affairs, the 
785board of registration in medicine, the bureau of health professions licensure, the office of the  38 of 119
786attorney general and other state agencies as appropriate. All such agencies shall provide data and 
787information necessary for the commission to create the plan.
788 (4) The state health plan shall include recommendations across a range of health care 
789services, including, but not limited to: (i) acute care; (ii) non-acute care; (iii) specialty care, 
790including, but not limited to, burn, coronary care, cancer care, neonatal care, post-obstetric and 
791post-operative recovery care, pulmonary care, renal dialysis and surgical, including trauma and 
792intensive care units; (iv) skilled nursing facilities; (v) assisted living facilities; (vi) long-term care 
793facilities; (vii) ambulatory 	surgical centers; (viii) office-based surgical centers; (ix) urgent care 
794centers; (x) home health; (xi) adult and pediatric behavioral health and mental health services 
795and supports; (xii) substance use disorder treatment and recovery services; (xiii) emergency care; 
796(xiv) ambulatory care services; (xv) primary care resources; (xvi) pediatric care services; (xvii) 
797pharmacy and pharmacological services; (xviii) family planning services; (xix) obstetrics and 
798gynecology and maternal health services; (xx) allied health services, including, but not limited 
799to, optometric care, chiropractic services, oral health care and midwifery services; (xxi) federally 
800qualified health centers and free clinics; (xxii) technologies or equipment defined as innovative 
801services or new technologies by the department of public health pursuant to section 25B of 
802chapter 111; (xxiii) hospice and palliative care service; (xxiv) health screening and early 
803intervention services; and (xxv) any other service or resource identified by the commission.
804 (5) The goal of the state health plan shall be to promote the appropriate and equitable 
805distribution of health care resources across geographic regions of the commonwealth based on 
806the needs of the population on a statewide basis and the needs of particular geographic and 
807demographic groups. The state health plan shall seek 	to support the commonwealth's goals of: (i) 
808maintaining and improving the quality of and access to health care services; (ii) ensuring a stable  39 of 119
809and adequate health care workforce; (iii) meeting the health care cost growth benchmark 
810established pursuant to section 9; (iv) supporting innovative health care delivery and alternative 
811payment models as identified by the commission; (v) reducing unnecessary duplication of health 
812care resources; (vi) advancing health equity and addressing disparities in the health care system 
813based on the needs of particular demographic factors, including, but not limited to, race, 
814ethnicity, immigration status, sexual orientation, gender identity, geographic location, age, 
815language spoken, ability and socioeconomic status; (vii) integrating oral health, mental health, 
816behavioral and substance use disorder treatment services with overall medical care; (viii) 
817aligning housing, health care and home care to improve overall health outcomes and reduce 
818costs; (ix) tracking trends in utilization and promoting the best standards of care; and (x) 
819ensuring equitable access to health care resources across geographic regions of the 
820commonwealth.
821 (6) The commission shall consult with the advisory council established pursuant to 
822section 4 in the development of the state health plan.
823 (7) In developing the state health plan, the commission, in consultation with the 
824department of public health, shall conduct at least 1 public hearing seeking input on the state 
825health plan and shall give interested persons an opportunity to submit their views orally and in 
826writing. In addition, the commission may create and maintain a website to allow members of the 
827public to submit comments electronically and review comments submitted by others. 
828 (8) The commission may require the submission of data and documents from providers, 
829provider organizations and payers to support creation of the state health plan; provided, that the 
830information is not already required to be reported to another state agency and accessible to the  40 of 119
831commission. Nonpublic clinical, financial, strategic or operational documents or information 
832provided to the commission in connection with this section shall be subject to section 2A.
833 (b)(1) In addition to the state health plan, the commission shall conduct regular, focused 
834assessments of provider supply and distribution in relation to projected need in at least 1 specific 
835service line. Each assessment shall be conducted in consultation with other state agencies as 
836appropriate, including, but not limited to, the executive office of health and human services, the 
837department of public health, the department of mental health, the office of Medicaid, the division 
838of insurance, the center for health information and analysis, the executive office of elder affairs, 
839the board of registration in medicine, the bureau of health professions licensure and the office of 
840the attorney general. All such agencies shall provide data and information necessary for the 
841commission to conduct the assessment. The commission shall consider available state and 
842national data and academic research on health service supply and need and relevant community 
843health needs assessments by non-profit hospitals and other organizations and other individual 
844and community statements of need.
845 (2) Each focused assessment shall examine at least 1 specific service line and at least 1 
846relevant region and may examine other factors in the public interest, such as populations served, 
847as appropriate. The service lines and regions shall be identified and prioritized for assessment by 
848the commission in consultation with the above-referenced agencies, as consistent with available 
849resources. In prioritizing service lines and regions, the commission may consider factors 
850including, but not limited to: (i) services with limited alternatives or substitutions; (ii) services 
851where supply has been shown to be misaligned with need nationally or in academic research; (iii) 
852services or regions undergoing significant changes in ownership, supply, or distribution; (iv) 
853services or regions with evidence of access challenges or barriers, particularly for vulnerable  41 of 119
854populations; (v) input from the advisory council established pursuant to section 4; and (vi) 
855requests for analysis from the executive office of health and human services or other agencies; 
856provided, that prioritized service lines under this paragraph shall include primary care and 
857behavioral health.
858 (3) Each assessment may include findings that include, but are not limited to: (i) the 
859extent to which supply of a given service line aligns with projected need at the statewide or 
860regional level; (ii) health system factors driving any documented health disparities; (iii) services 
861or providers, including in a specific geographic area, that are critical to the proper functioning of 
862the health care system; (iv) estimates of where and how many additional units of service would 
863be needed in the state or in a specific geographic area to meet projected need; (v) identification 
864of barriers impacting accessibility of available supply by specific populations; and (vi) policy 
865recommendations to address the drivers of disparities, access barriers and areas of misalignment 
866of need and supply.
867 (4) The commission shall consult with the advisory council established pursuant to 
868section 4 in the development of such focused assessments.
869 (5) The commission, in consultation with the department of public health, shall conduct 
870at least 1 public hearing seeking input on each focused assessment and shall give interested 
871persons an opportunity to submit testimony orally and in writing.
872 (6) The commission may require the submission of data and documents from payers, 
873providers or provider organizations that offer a service that is the subject of an assessment 
874conducted under this section; provided, that the information is not already reported to another 
875state agency and made accessible to the commission. 	Nonpublic clinical, financial, strategic or  42 of 119
876operational documents or information provided to the commission in connection with this section 
877shall be subject to section 2A.
878 (c) The commission shall publish analyses, reports and interpretations of information 
879collected pursuant to this section to promote awareness of the distribution and nature of health 
880care resources in the commonwealth.
881 (d) Biennially, not later than January 1, the commission shall file a report with the joint 
882committee on health care financing , which shall include, but not be limited to: (i) a summary of 
883the current state health plan and a description of focused assessments conducted during the past 2 
884years; (ii) a summary of actions taken by the commission and progress made toward developing 
885the state health plan and focused assessments during the past 2 years; and (iii) recommendations 
886for further legislative action to assist the commission in its implementation of this section.
887 Section 23. (a) A provider or a provider organization in which a private equity firm has a 
888financial interest shall not: (i) meet or exceed the maximum adjusted debt to adjusted EBITDA 
889ratio; (ii) otherwise become highly leveraged, as determined by the commission; (iii) transact 
890with an unsafe financial actor; (iv) for the period during which the private equity firm has a 
891financial interest in the provider or provider organization, (A) provide capital distributions, 
892including, but not limited, to cash dividends, stock dividends that are not strictly dilutive or any 
893other similar distributions, (B) perform stock buybacks, stock redemptions or similar transactions 
894or (C) pay to a private equity firm management fees or similar fees or costs; or (v) perform any 
895other action or exceed any other metric the commission determines may cause a provider or 
896provider organization to become financially distressed.  43 of 119
897 (b) Within 30 days 	of the commission receiving a referral from the center pursuant to 
898paragraph (4) of subsection (e) of section 9 of chapter 12C or the commission becoming aware of 
899a potential violation of subsection (a) pursuant to the 	filing of a completed notice of material 
900change under section 13, the commission shall make a determination of whether there has been a 
901violation. If the commission determines a violation has occurred, the commission shall require 
902the provider to come into compliance with said subsection (a) and may set conditions that the 
903provider or provider organization shall follow to come into compliance. The commission shall 
904notify the provider or provider organization in writing of its determination, conditions, if any, 
905and reasoning. The provider or provider organization shall have not less than 30 days to respond 
906in writing and 10 days to request a hearing from the date of notification. If a hearing is requested, 
907the hearing shall be held within 30 days of the commission’s receipt of the request. Within 10 
908days of receiving written comments or holding any requested hearing, whichever is later, the 
909commission shall notify the provider or provider organization in writing that the provider or 
910provider organization is required to come into compliance with section (a) and which conditions, 
911if any, shall go into effect. Upon providing notice, such requirements and conditions, if any, shall 
912go into effect. 
913 In making the determinations pursuant to subsection (a), the commission may consider all 
914publicly available data and documents, including information submitted to the commission and 
915the center under any authority. The commission may also solicit additional non-public 
916information from providers to the extent necessary to achieve the purposes of this section. The 
917commission shall keep confidential all nonpublic information and documents obtained under this 
918section, and such information shall not be public records and shall be exempt from disclosure 
919under clause Twenty-sixth of section 7 of chapter 4 or section 10 of chapter 66.  44 of 119
920 (c)(1) Within 3 months, or a shorter reasonable time as determined by the commission, 
921the commission shall determine whether the provider or provider organization has substantially 
922complied with its conditions or if no conditions were set, whether the provider or provider 
923organization has come into compliance with subsection (a). The commission shall notify the 
924provider or provider organization of its determination and reasoning, and the provider or 
925provider organization shall have not less than 30 days to respond in writing and 10 days to 
926request a hearing from the date of notification. If a hearing is requested, the hearing shall be held 
927within 30 days of the commission’s receipt of the request. Within 10 days of receiving written 
928comments and holding any requested hearing, whichever is later, the commission shall make a 
929final determination and notify the provider or provider organization of the determination in 
930writing.
931 (2) If the commission makes a final determination that the provider or provider 
932organization has failed to substantially implement the commission’s conditions, or, if no 
933conditions were set, to come in compliance with subsection (a), the department of public health 
934may collect the bond deposited. The commission shall notify the department of public health of 
935its determination and refer the provider or provider organization to the attorney general. 
936 (3) Failure to substantially implement the commission’s conditions, or, if no conditions 
937are set, failure to come in compliance with subsection (a) shall constitute a violation of said 
938chapter 93A. Only the attorney general, or an organization representing workers who: (i) worked 
939for the provider or provider organization; (ii) worked in the provider or provider organization’s 
940facilities, if any; or (iii) contracted with the provider or provider organization, may bring an 
941action under chapter 93A for such a violation. The commission’s final determination may be 
942used as prima facie evidence of a violation of said chapter 93A. 45 of 119
943 (d) A private equity firm shall deposit, upon submission of a notice of material change 
944pursuant to section 13 of chapter 6D, a bond with the department of public health ensuring that 
945the provisions of subsection (a) shall not be violated; provided, however, that the private equity 
946firm shall not use any of the provider or provider organization’s assets or property as security for 
947the bond, pay for the bond by placing debt on the provider or provider organization or otherwise 
948permit the provider or provider organization to pay the bond on the private equity firm’s behalf 
949or allow the provider or provider organization to be liable for the bond. 
950 SECTION 33. Section 5A of chapter 12 of the General Laws, as so appearing, is hereby 
951amended by striking out, in line 26, the words “or ‘knowingly’” and inserting in place thereof the 
952following words:- , “knowingly” or “knows”.
953 SECTION 34. Said section 5A of said chapter 12, as so appearing, is hereby further 
954amended by inserting after the definition of “Overpayment” the following definition:-
955 “Ownership or investment interest”, any: (1) direct or indirect possession of equity in the 
956capital, stock or profits totaling more than 10 per cent of an entity; (2) interest held by an 
957investor or group of investors who engages in the raising or returning of capital and who invests, 
958develops or disposes of specified assets; (3) interest held by a pool of funds by investors, 
959including a pool of funds managed or controlled by private limited partnerships, if those 
960investors or the management of that pool or private limited partnership employ investment 
961strategies of any kind to earn a return on that pool of funds; or (4) interest held by a real estate 
962investment trust.
963 SECTION 35. Section 5B of said chapter 12, as so appearing, is hereby amended by 
964striking out, in line 29, the word “or”, the second time it appears. 46 of 119
965 SECTION 36. Said section 5B of said chapter 12, as so appearing, is hereby further 
966amended by inserting after the word “applicable”, in lines 38 and 39, the following words:- ; or 
967(11) has an ownership or investment interest in any person who violates clauses (1) to (10), 
968inclusive, knows about the violation, and fails to disclose the violation to the commonwealth or a 
969political subdivision thereof within 60 days of identifying the violation.
970 SECTION 37. Section 11N of said chapter 12, as so appearing, is hereby amended by 
971striking out, in line 7, the words “or provider organization” and inserting in place thereof the 
972following words:- , provider organization, private equity firm, real estate investment trust, 
973management services organization, pharmaceutical manufacturing company and pharmacy 
974benefit manager.
975 SECTION 38. Said section 11N of said chapter 12, as so appearing, is hereby further 
976amended by striking out subsection (b) and inserting in place thereof the following subsection:- 
977 (b) The attorney general may investigate any provider organization referred to the 
978attorney general by the health policy commission under chapter 6D to determine whether the 
979provider organization engaged in unfair methods of competition or anti-competitive behavior in 
980violation of chapter 93A or any other law, and, if appropriate, take action under said chapter 93A 
981or any other law to protect consumers in the health care market, including, but not limited to, an 
982action for injunctive relief.
983 SECTION 39. Section 1 of chapter 12C of the General Laws, as so appearing, is hereby 
984amended by inserting after the definition of “Ambulatory surgical center services” the following 
985definition:- 47 of 119
986 “Benchmark cycle”, a period of 2 consecutive calendar years during which the projected 
987annualized growth rate in total health care expenditures in the commonwealth is calculated 
988pursuant to section 9 of chapter 6D and monitored pursuant to section 10 of said chapter 6D.
989 SECTION 40. Said section 1 of said chapter 12C, as so appearing, is hereby further 
990amended by inserting after the definition of “Fee-for-service” the following definition:-
991 “Financial interest”, when a private equity firm or its corporate affiliate has a direct or 
992indirect ownership share of, or controlling interest in, or is a holder of significant debt from a 
993provider or provider organization or the provider or provider organization’s corporate affiliates
994 SECTION 41. Said section 1 of said chapter 12C, as so appearing, is hereby further 
995amended by striking out the definition of “Health care cost growth benchmark” and inserting in 
996place thereof the following 2 definitions:-
997 “Health care cost growth benchmark”, the projected annualized growth rate in total health 
998care expenditures in the commonwealth during a benchmark cycle as established in section 9 of 
999chapter 6D.
1000 “Health care entity”, as defined in section 1 of chapter 6D.
1001 SECTION 42. Said section 1 of said chapter 12C, as so appearing, is hereby further 
1002amended by inserting after the definition of “Health care services” the following 2 definitions:-
1003 “Health disparities”, preventable differences in the burden of disease, injury, violence or 
1004opportunities to achieve optimal health that are experienced by socially disadvantaged 
1005populations.  48 of 119
1006 “Health equity”, the state in which a health system offers the infrastructure, facilities, 
1007services, geographic coverage, affordability and all other relevant features, conditions and 
1008capabilities that will provide all people with the opportunity and reasonable expectation that they 
1009can reach their full health potential and well-being and are not disadvantaged in access to health 
1010care by their race, ethnicity, language, disability, age, gender, gender identity, sexual orientation, 
1011social class, intersections among these communities or identities or their socially determined 
1012circumstances.
1013 SECTION 43. Said section 1 of said chapter 12C, as so appearing, is hereby further 
1014amended by inserting after the definition of “Major service category” the following 2 
1015definitions:- 
1016 “Management services organization”, a business that provides management or 
1017administrative services to a provider or provider organization for compensation.	“Maximum 
1018adjusted debt to adjusted EBITDA ratio”, the highest 	ratio of total adjusted debt to adjusted 
1019earnings before interest, taxes, depreciation and amortization the commission determines that a 
1020provider or provider organization can have without becoming financially unstable; provided 
1021further, that the commission, in consultation with the center, shall establish a standard method of 
1022calculating and reporting total adjusted debt and adjusted earnings before interest, taxes, 
1023depreciation and amortization; and provided further, that the methodology and reporting shall 
1024include capitalized lease obligations.
1025 SECTION 44. Said section 1 of said chapter 12C, as so appearing, is hereby further 
1026amended by inserting after the definition of “Patient-centered medical home” the following 3 
1027definitions:- 49 of 119
1028 “Payer”, any entity, other than an individual, that pays providers for the provision of 
1029health care services; provided, that “payer” shall include both governmental and private entities; 
1030provided further, that “payer” shall include self-insured plans to the extent allowed under the 
1031federal Employee Retirement Income Security Act of 1974.
1032 “Pharmaceutical manufacturing company”, an entity engaged in the: (i) production, 
1033preparation, propagation, compounding, conversion or processing of prescription drugs, directly 
1034or indirectly, by extraction from substances of natural origin, independently by means of 
1035chemical synthesis or by a combination of extraction and chemical synthesis; or (ii) packaging, 
1036repackaging, labeling, relabeling or distribution of prescription drugs; provided, however, that 
1037“pharmaceutical manufacturing company” shall not include a wholesale drug distributor licensed 
1038under section 36B of chapter 112 or a retail pharmacist registered under section 39 of said 
1039chapter 112.
1040 “Pharmacy benefit manager”, a person, business or other entity, however organized, that, 
1041directly or through a subsidiary, provides pharmacy benefit management services for prescription 
1042drugs and devices on behalf of a health benefit plan sponsor, including, but not limited to, a self-
1043insurance plan, labor union or other third-party payer; provided, however, that pharmacy benefit 
1044management services shall include, but not be limited to: (i) the processing and payment of 
1045claims for prescription drugs; (ii) the performance of drug utilization review; (iii) the processing 
1046of drug prior authorization requests; (iv) pharmacy contracting; (v) the adjudication of appeals or 
1047grievances related to prescription drug coverage contracts; (vi) formulary administration; (vii) 
1048drug benefit design; (viii) mail and specialty drug pharmacy services; (ix) cost containment; (x) 
1049clinical, safety and adherence programs for pharmacy services; and (xi) managing the cost of 
1050covered prescription drugs; provided further, that “pharmacy benefit manager” shall include a  50 of 119
1051health benefit plan sponsor that does not contract with a pharmacy benefit manager and manages 
1052its own prescription drug benefits unless specifically exempted by the commission.
1053 SECTION 45. Said section 1 of said chapter 12C, as so appearing, is hereby further 
1054amended by inserting after the definition of “Primary service area” the following definition:-
1055 “Private equity firm”, a publicly traded or non-publicly traded company that collects 
1056capital investments from individuals or entities and purchases, as a parent company or through 
1057another entity that it completely or partially owns or controls, a direct or indirect ownership share 
1058of or controlling interest in, or otherwise obtains a financial interest in, a provider, provider 
1059organization or management services organization; provided, however, that “private equity firm” 
1060shall not include venture capital firms exclusively funding startups or other early-stage 
1061businesses.
1062 SECTION 46. Said section 1 of said chapter 12C, as so appearing, is hereby further 
1063amended by striking out the definition of “Provider organization” and inserting in place thereof 
1064the following definition:-
1065 “Provider organization”, any corporation, partnership, business trust, association or 
1066organized group of persons, which is in the business of health care delivery or management, 
1067whether incorporated or not, that represents at least 1 health care providers in contracting with 
1068carriers, third party administrators or public payers for the payments of health care services; 
1069provided, that ''provider organization'' shall include, but not be limited to, physician 
1070organizations, physician-hospital organizations, independent practice associations, provider 
1071networks, accountable care organizations, management services organizations, providers that are 
1072owned or controlled, fully or partially, by for-profit entities, including, but not limited to, private  51 of 119
1073equity firms, and any other organization that contracts with carriers, third party administrators or 
1074public payers for payment for health care services; and provided, further that “provider 
1075organization” shall not include any integrated care network that is owned and directed by a long-
1076term care providers. 
1077 SECTION 47. Said section 1 of said chapter 12C, as so appearing, is hereby further 
1078amended by inserting after the definition of “Quality measures” the following definition:-
1079 “Real estate investment trust”, a real estate investment trust as defined in 26 U.S.C. 856.
1080 SECTION 48. Said section 1 of said chapter 12C, as so appearing, is hereby further 
1081amended by inserting after the definition of “Total health care expenditures” the following 2 
1082definitions:-
1083 “Total medical expenses”, the total cost of care for the patient population associated with 
1084a provider organization based on allowed claims for all categories of medical expenses and all 
1085non-claims related payments to providers.
1086 “Unsafe financial actor”, a private equity firm or real estate investment trust that had a 
1087financial interest in a provider or provider organization closing, declaring bankruptcy or 
1088otherwise discontinuing its operations within 15 years of the private equity firm or real estate 
1089investment trust’s financial interest in the provider or provider organization.
1090 SECTION 49. Section 2A of said chapter 12C, as so appearing, is hereby amended by 
1091inserting after the word “cybersecurity”, in line 9, the following words:- and 1 of whom shall 
1092have experience in health equity advocacy. 52 of 119
1093 SECTION 50. Section 3 of said chapter 12C, as so appearing, is hereby amended by 
1094striking out, in line 11, the word “benchmark” and inserting in place thereof the following 
1095words:- and affordability benchmarks.
1096 SECTION 51. Said section 3 of said chapter 12C, as so appearing, is hereby further 
1097amended by striking out, in line 12, the words “section 9” and inserting in place thereof the 
1098following words:- sections 9 and 9A.
1099 SECTION 52. The 	first paragraph of section 7 of said chapter 12C, as so appearing, is 
1100hereby amended by adding the following sentence:- 
1101 Each pharmaceutical manufacturing company and pharmacy benefit manager shall pay to 
1102the commonwealth an amount for the estimated expenses of the center and for the other purposes 
1103described in this chapter.
1104 SECTION 53. Said section 7 of said chapter 12C, as so appearing, is hereby further 
1105amended by striking out, in lines 8 and 42, the figure “33” and inserting in place thereof, in each 
1106instance, the following figure:- “25”.
1107 SECTION 54. Said section 7 of said chapter 12C, as so appearing, is hereby further 
1108amended by adding following 3 paragraphs:- To the maximum extent under federal law, 
1109provided that such assessment shall not result in any reduction of federal financial participation 
1110in Medicaid, the assessed amount for pharmaceutical manufacturing companies shall be not less 
1111than 25 per cent of the amount appropriated by the general court for the expenses of the center 
1112minus amounts collected from: (i) filing fees; (ii) fees and charges generated by the center's 
1113publication or dissemination of reports and information; and (iii) federal matching revenues 
1114received for these expenses or received retroactively for expenses of predecessor agencies.  53 of 119
1115Pharmaceutical manufacturing companies shall pay such assessed amount multiplied by the ratio 
1116of the pharmaceutical manufacturing company’s gross sales of outpatient prescription drugs 
1117dispensed in the commonwealth or similar measure determined by the center consistent with 
1118applicable federal requirements. 
1119 To fund the operations of the licensure of pharmacy benefit managers to the maximum 
1120extent allowed by federal law and to the extent that the assessment will not result in any 
1121reduction of federal financial participation in Medicaid, the assessed amount for pharmacy 
1122benefit managers shall be not less than 25 per cent of the amount appropriated by the general 
1123court for the expenses of the center minus amounts collected from: (i) filing fees; (ii) fees and 
1124charges generated by the center's publication or dissemination of reports and information; and 
1125(iii) federal matching revenues received for these expenses or received retroactively for expenses 
1126of predecessor agencies. Pharmacy benefit managers shall pay such assessed amount multiplied 
1127by the ratio of the pharmacy benefit manager’s gross revenue related to outpatient prescription 
1128drugs dispensed in the commonwealth or similar measure determined by the center consistent 
1129with applicable federal requirements. In no event may this assessment, when combined with the 
1130assessment of pharmacy benefit managers in section 6 of chapter 6D and the pharmacy benefit 
1131manager licensing fee in section 2 of chapter 176Y, exceed the commonwealth’s estimated 
1132expense in operating the pharmacy benefit manager licensure program. Each pharmaceutical 
1133manufacturing company and each pharmacy benefit manager shall make a preliminary payment 
1134to the center on October 1 of each year in an amount equal to 1/2 of the initial year’s and, 
1135subsequently, the previous year's total assessment. Thereafter, each pharmaceutical 
1136manufacturing company and each pharmacy benefit manager shall pay, within 30 days’ notice  54 of 119
1137from the center, the balance of the total assessment for the current year as determined by the 
1138center. 
1139 SECTION 55. Section 8 of said chapter 12C, as so appearing, is hereby amended by 
1140inserting after the word “entities”, in line 5, the following words:- , including, but not limited to, 
1141private equity firms, real estate investment trusts and management services organizations.
1142 SECTION 56. Said section 8 of said chapter 12C, as so appearing, is hereby further 
1143amended by inserting after the word “statements”, in line 23, the following words:- , including 
1144the audited financial statements of the parent organization’s out-of-state operations, private 
1145equity firms, real estate investment trusts and management services organizations,.
1146 SECTION 57. Said section 8 of said chapter 12C, as so appearing, is hereby further 
1147amended by striking out, in line 49, the words “and (6)” and inserting in place thereof the 
1148following words:- (6) investments; and (7) information on any relationships with private equity 
1149firms, real estate investment trusts and management services organizations; and (8).
1150 SECTION 58. Said chapter 12C is hereby further amended by striking out section 9, as so 
1151appearing, and inserting in place thereof the following section:- 
1152 Section 9. (a) The center, in consultation with the commission, shall promulgate 
1153regulations to require that provider organizations registered under section 11 of chapter 6D 
1154annually report the data as the center considers necessary to better protect the public interest in 
1155monitoring the financial conditions, organizational structure, business practices, clinical services 
1156and market share of each registered provider organization. The center may assess administrative 
1157fees on provider organizations in an amount to help defray the center's costs in complying with  55 of 119
1158this section. The center may specify in regulations uniform reporting standards and reporting 
1159thresholds as it determines necessary. 
1160 (b) The center shall require registered provider organizations to report information 
1161necessary to achieve the goals described in subsection (a), which may include, but shall not be 
1162limited to: (i) organizational charts showing the ownership, governance and operational structure 
1163of the provider organization, including any clinical affiliations and community advisory boards; 
1164(ii) the number of affiliated health care professional full-time equivalents by license type, 
1165specialty, name and address of practice locations and whether the professional is employed by 
1166the organization; (iii) the name and address of licensed facilities by license number, license type 
1167and capacity in each major service category; (iv) the name, address and capacity of all other 
1168locations where the provider organization, or any of its affiliates, delivers health care services, 
1169including those services listed in paragraph (4) of subsection (a) of section 22 of chapter 6D; (v) 
1170counts and capacity estimates of health care equipment as defined by the center, including 
1171imaging equipment; (vi) a comprehensive financial statement, including information on parent 
1172entities, including their out-of-state operations, and corporate affiliates, including private equity 
1173firms, real estate investment trusts and management services organizations, as applicable, and 
1174including details regarding annual costs, annual receipts, realized capital gains and losses, 
1175accumulated surplus and accumulated reserves; (vii) information on stop-loss insurance and any 
1176non-fee-for-service payment arrangements; (viii) information on clinical quality, care 
1177coordination and patient referral practices; (ix) information regarding expenditures and funding 
1178sources for payroll, teaching, research, advertising, taxes or payments-in-lieu-of-taxes and other 
1179non-clinical functions; (x) information regarding charitable care and community benefit 
1180programs; (xi) for any risk-bearing provider organization, a certificate from the division of  56 of 119
1181insurance under chapter 176U; (xii) information regarding other assets and liabilities that may 
1182affect the financial condition of the provider organization or the provider organization’s 
1183facilities, including, but not limited to, real estate sale-leaseback arrangements with real estate 
1184investment trusts; and (xiii) such other information as the center considers appropriate as set 
1185forth in the center's regulations; provided, however, that the center shall coordinate with the 
1186commission and the division of insurance to obtain information directly from the commission; 
1187provided further, that the center shall consider the administrative burden of reporting when 
1188developing reporting requirements. The center may, in consultation with the division of 
1189insurance and the commission, merge similar reporting requirements where appropriate. The 
1190center, in its discretion, may specify additional data elements in a given reporting year to support 
1191the development of the state health plan or the focused assessments defined in said section 22 of 
1192said chapter 6D. 
1193 (c) Annual reporting shall be in a form provided by the center. The center shall 
1194promulgate regulations that define criteria for waivers from certain annual reporting 
1195requirements under this section. Criteria for waivers may include operational size of the provider 
1196organization, the provider organization's annual net patient service revenue, the degree of risk 
1197assumed by the provider organization and other criteria as the center considers appropriate. 
1198 (d) Notwithstanding the annual reporting requirements under this section, the center may 
1199require in writing, at any time, additional information that is reasonable and necessary to 
1200determine the financial condition, organizational structure, business practices, clinical services or 
1201market share of a registered provider organization. 57 of 119
1202 (e) The center shall develop and maintain an inventory of health care resources on its 
1203website in a form usable by the public; provided, that the extracts must include information on 
1204the geographic distribution of clinicians, facilities, equipment or any other health care resources. 
1205Such inventory shall be derived from all available data, including, but not limited to, data 
1206collected under this section and data collected by other state agencies. Agencies that license, 
1207register, regulate or otherwise collect cost, quality or other data concerning health care resources 
1208shall provide the center and the commission such data and information necessary to develop and 
1209maintain the inventory required by this this section. 
1210 (f) The center may enter into interagency agreements with the commission and other state 
1211agencies to effectuate the goals of this section.
1212 (g)(1) The center shall also collect and analyze such data as it considers necessary to 
1213protect the public interest in monitoring financial conditions of registered provider organizations 
1214and compliance with subsection (a) of section 23 of chapter 6D by registered provider 
1215organizations with private equity investment. To effectuate this subsection, the center may: (i) 
1216modify uniform reporting requirements; (ii) require registered provider organizations with 
1217private equity investment to report required information quarterly; (iii) require relevant 
1218information from private equity firms and their affiliates; and (iv) communicate confidentially 
1219with registered provider organizations as the center deems necessary. 
1220 (2) The information shall be analyzed on an industry-wide and provider-specific basis 
1221and shall include, but not be limited to: (i) gross and net patient service revenues; (ii) sources of 
1222revenue; (iii) total payroll as a per cent of operating expenses and the salary and benefits of the  58 of 119
1223top 10 highest compensated employees, identified by position description and specialty; and (iv) 
1224other relevant measures of financial health or distress. 
1225 (3) The center shall publish annual reports and establish a continuing program of 
1226investigation and study of financial trends among registered provider organizations, including an 
1227analysis of systemic instabilities or inefficiencies that contribute to financial distress. The reports 
1228shall include an identification and examination of: (i) 	registered provider organizations that the 
1229center considers to be in financial distress, including any at risk of closing or discontinuing 
1230essential health services, as defined by the department of public health under section 51G of 
1231chapter 111, as a result of financial distress; and (ii) registered provider organizations with 
1232private equity investment that have violated subsection (a) of section 23 of chapter 6D. The 
1233center may provide this information in the report it produces pursuant to subsection (c) of section 
12348.
1235 (4) The center shall refer to the commission any provider in which a private equity firm 
1236has a financial interest that has violated subsection (a) of section 23 of chapter 6D.
1237 SECTION 59. Section 10 of said chapter 12C, as so appearing, is hereby amended by 
1238inserting after the word “of”, in line 21, the following words:- communities and purchaser.
1239 SECTION 60. Subsection (b) of said section 10 of chapter 12C, as so appearing, is 
1240hereby further amended by striking out clause (8) and inserting in place thereof the following 
1241clause:- 
1242 (8) relative prices paid to every hospital or physician group in the payer’s network, by 
1243type of provider, with hospital inpatient and outpatient prices listed separately and product type, 
1244including health maintenance organization and preferred provider organization products. 59 of 119
1245 SECTION 61. Said subsection (b) of said section 10 of said chapter 12C, as so appearing, 
1246is hereby further amended by striking out, in lines 56 to 61, inclusive, the words “and (11) a 
1247comparison of relative prices for the payer’s participating health care providers by provider type 
1248which shows the average relative price, the extent of variation in price, stated as a percentage, 
1249and identifies providers who are paid more than 10 per cent, 15 per cent and 20 per cent above 
1250and more than 10 per cent, 15 per cent and 20 per cent below the average relative price” and 
1251inserting in place thereof the following words:- (11) information about prescription drug 
1252utilization and spending for all covered drugs, including for generic drugs, brand-name drugs and 
1253specialty drugs provided in an inpatient or outpatient setting or sold in a retail setting, including, 
1254but not limited to, information sufficient to show the: (i) highest utilization drugs, (ii) drugs with 
1255the greatest increases in utilization, (iii) drugs that are most impactful on plan spending, net of 
1256rebates, (iv) drugs with the highest year-over-year price increases, net of rebates, and (v) drugs 
1257with the highest cost per prescription both gross and net of rebates; (12) information on clinical 
1258quality, care coordination and patient referral practices; and (13) a comparison of relative prices 
1259for the payer’s participating health care providers by provider type, which shows the average 
1260relative price and the extent of variation in price and identifies providers who are paid more than 
126110 per cent, 15 per cent and 20 per cent above and more than 10 per cent, 15 per cent and 20 per 
1262cent below the average relative price.
1263 SECTION 62. Subsection (c) of said section 10 of said chapter 12C, as so appearing. is 
1264hereby amended by striking out clause (8) and inserting in place thereof the following clause:-
1265 (8) relative prices paid to every hospital or physician group in the payer’s network, by 
1266type of provider, with hospital inpatient and outpatient prices listed separately and product type, 
1267including health maintenance organization and preferred provider organization products. 60 of 119
1268 SECTION 63. Said subsection (c) of said section 10 of said chapter 12C, as so appearing, 
1269is hereby further amended by striking out, in lines 99 to 104, inclusive, the words “and (11) a 
1270comparison of relative prices for the payer’s participating health care providers by provider type 
1271which shows the average relative price, the extent of variation in price, stated as a percentage and 
1272identifies providers who are paid more than 10 per cent, 15 per cent and 20 per cent above and 
1273more than 10 per cent, 15 per cent and 20 per cent below the average relative price” and inserting 
1274in place thereof the following words:- (11) information about prescription drug utilization and 
1275spending for all covered drugs, including for generic drugs, brand-name drugs and specialty 
1276drugs provided in an inpatient or outpatient setting or sold in a retail setting, including, but not 
1277limited to, information sufficient to show the: (i) highest utilization drugs, (ii) drugs with the 
1278greatest increases in utilization, (iii) drugs that are most impactful on plan spending, net of 
1279rebates, (v) drugs with the highest year-over-year price increases, net of rebates, and (v) drugs 
1280with the highest cost per prescription, both gross and net of rebates; (12) information on clinical 
1281quality, care coordination and patient referral practices; and (13) a comparison of relative prices 
1282for the payer’s participating health care providers by provider type, which shows the average 
1283relative price and the extent of variation in price and identifies providers who are paid more than 
128410 per cent, 15 per cent and 20 per cent above and more than 10 per cent, 15 per cent and 20 per 
1285cent below the average relative price.
1286 SECTION 64. Said chapter 12C is hereby amended by inserting after section 10 the 
1287following section:- 
1288 Section 10A. (a) The center shall promulgate regulations necessary to ensure the uniform 
1289annual reporting of information from pharmacy benefit managers certified under chapter 176Y, 
1290including, but not limited to, data from the most recent calendar year detailing: (i) all discounts,  61 of 119
1291including the total dollar amount and percentage discount and rebates received from a 
1292manufacturer for each drug on the pharmacy benefit manager's formularies; (ii) the total dollar 
1293amount of all discounts and rebates that are retained by the pharmacy benefit manager for each 
1294drug on the pharmacy benefit manager's formularies; (iii) actual total reimbursement amounts for 
1295each drug the pharmacy benefit manager pays retail pharmacies after all direct and indirect 
1296administrative and other fees that have been retrospectively charged to the pharmacies are 
1297applied; (iv) the negotiated price health plans pay the pharmacy benefit manager for each drug 
1298on the pharmacy benefit manager's formularies; (v) the amount, terms and conditions relating to 
1299copayments, reimbursement options and other payments or fees associated with a prescription 
1300drug benefit plan; and (vi) disclosure of any ownership interest the pharmacy benefit manager 
1301has in a pharmacy or health plan with which it conducts business or any corporate affiliation 
1302between the pharmacy benefit manager and the pharmacy or health plan with which it conducts 
1303business; provided, however, that the center may examine or audit the financial records of a 
1304pharmacy benefit manager 	for purposes of ensuring the information submitted pursuant to 
1305regulations promulgated under this section is accurate.  
1306 (b) The center shall analyze the information and data collected under subsection (a) and 
1307shall publish an annual report summarizing, at minimum, the information collected under said 
1308subsection (a) and comparing the information as it relates to pharmacy benefit managers certified 
1309under chapter 176Y with respect to drugs provided to residents of the commonwealth. 
1310 (c) Except as specifically provided otherwise by the center or under this chapter, 
1311pharmacy benefit manager 	data collected by the center under this section shall not be a public 
1312record under clause Twenty-sixth of section 7 of chapter 4 or chapter 66. The center may  62 of 119
1313confidentially provide pharmacy benefit manager data collected by the center under this section 
1314to the health policy commission.
1315 SECTION 65. Said chapter 12C is hereby further amended by striking out section 11, as 
1316appearing in the 2022 Official Edition, and inserting in place thereof the following section:-
1317 Section 11. The center shall ensure the timely reporting of information required under 
1318sections 8 to 10, inclusive. The center shall notify entities required to submit data under this 
1319chapter of any applicable reporting deadlines. The center shall notify, in writing, an entity, other 
1320than a public payer required to submit data under this chapter, which has failed to meet a 
1321reporting deadline and that failure to respond within 2 weeks of the receipt of the notice may 
1322result in penalties. The center may assess a penalty against an entity other than a public health 
1323care payer required to submit data under this chapter that fails, without just cause, to provide the 
1324requested information within 2 weeks following receipt of the written notice required under this 
1325paragraph, of not more than $25,000 per week for each week of delay after the 2-week period 
1326following the reporting entity’s receipt of the written notice. Amounts collected under this 
1327section shall be deposited in the Healthcare Payment Reform Fund, established under section 100 
1328of 194 of the acts of 2011. The center shall notify the commission and the department of public 
1329health if a provider or provider organization fails to timely report in accordance with this section, 
1330or if the center has assessed a penalty under this section. Such notification shall be considered by 
1331the commission in a cost and market impact review under section 13 of chapter 6D, and by the 
1332department in determining licensure and suitability in accordance with section 51 of chapter 111 
1333and for a determination of need under section 25C of said chapter 111. 63 of 119
1334 SECTION 66. Section 12 of said chapter 12C, as so appearing, is hereby amended by 
1335adding the following subsection:-
1336 (c) Notwithstanding any general or special law to the contrary, a provider, private health 
1337care payer, public health care payer, agency, department, division, commission, board, authority 
1338or other public or quasi-public entity in the commonwealth that collects patient information, 
1339including personal data as defined in section 1 of chapter 66A, shall, upon a request from the 
1340center, provide such data to the center for any purpose consistent with this chapter; provided, 
1341however, that the disclosure of such information shall be in compliance with federal law.
1342 SECTION 67. Said chapter 12C is hereby further amended by striking out section 14, as 
1343so appearing, and inserting in place thereof the following section:- 
1344 Section 14. (a)(1) Not later than March 1 in each even-numbered year, the center, in 
1345consultation with the statewide advisory committee established pursuant to subsection (c), shall 
1346establish a standard set of measures of health care provider quality and health system 
1347performance, hereinafter referred to as the “standard quality measure set”, for use in: (i) contracts 
1348between payers, including between the commonwealth and carriers and between health care 
1349providers, provider organizations and accountable care organizations, which incorporate quality 
1350measures into payment terms, including the designation of a set of core measures and a set of 
1351non-core measures; (ii) assigning tiers to health care providers in the design of any health plan; 
1352(iii) consumer transparency websites and other methods of providing consumer information; (iv) 
1353monitoring system-wide performance; and (v) reducing provider administrative burden related to 
1354quality measure reporting.  64 of 119
1355 (2) The standard quality measure set shall designate: (i) core measures that shall be used 
1356in contracts that incorporate quality measures into payment terms between payers, including the 
1357commonwealth and carriers, and health care providers, including provider organizations and 
1358accountable care organizations, and shall meet the core criteria set by the statewide advisory 
1359committee pursuant to paragraph (3) of subsection (c); and (ii) a menu of non-core measures that 
1360may be used in such contracts. The standard quality measure set shall allow for innovation and 
1361the development of outcome measures for quality and safety. If the standard quality measure set 
1362established by the center differs from the recommendations of the statewide advisory committee, 
1363the center shall issue a written report detailing each area of disagreement and the rationale for the 
1364center’s decision.
1365 (b) The center shall develop uniform reporting requirements for the standard quality 
1366measure set for each health care provider facility, medical group or provider group in the 
1367commonwealth; provided, however, that the center shall prioritize the development of uniform 
1368reporting requirements for primary care and behavioral health providers; and provided further, 
1369that the uniform reporting requirements shall not increase provider administrative burden related 
1370to quality measure reporting.
1371 (c)(1) The center shall convene a statewide advisory committee which shall make 
1372recommendations for the standard quality measure set to: (i) ensure consistency in the use of 
1373quality and safety measures in contracts between payers, including the commonwealth and 
1374carriers, and health care providers in the commonwealth; (ii) ensure consistency in methods for 
1375the assignment of tiers to providers in the design of any health plan; (iii) improve quality and 
1376safety of care; (iv) improve transparency for consumers and employers; (v) improve health  65 of 119
1377system monitoring and oversight by relevant state agencies; and (vi) reduce administrative 
1378burdens.
1379 (2) The statewide advisory committee shall consist of commissioner of insurance or a 
1380designee, who shall serve as co-chair; the executive director of the health policy commission, or 
1381their designee, who shall serve as co-chair; the executive director of the center; the executive 
1382director of the Betsy Lehman center for patient safety and medical error reduction; the executive 
1383director of the group insurance commission; the secretary of elder affairs; the assistant secretary 
1384for MassHealth; the commissioner of the department of public health; the commissioner of the 
1385department of mental health; and 11 members who shall be appointed by the governor, 1 of 
1386whom shall be a representative of Massachusetts Health and Hospital Association, Inc., 1 of 
1387whom shall be a representative of the Massachusetts League of Community Health Centers, Inc., 
13881 of whom shall be a representative the Massachusetts Medical Society, 1 of whom shall be a 
1389registered nurse licensed to practice in the commonwealth who practices in a patient care setting, 
13901 of whom shall be a representative of a labor organization representing health care workers, 1 of 
1391whom shall be a behavioral health provider, 1 of whom shall be a long-term supports and 
1392services provider, 1 of whom shall be a representative of Blue Cross and Blue Shield of 
1393Massachusetts, Inc., 1 of whom shall be a representative of Massachusetts Association of Health 
1394Plans, Inc., 1 of whom shall be a representative of a specialty pediatric provider and 1 of whom 
1395shall be a representative of consumers. Members appointed to the statewide advisory committee 
1396shall have experience with and expertise in health care quality measurement.
1397 (3) The statewide advisory committee shall meet quarterly to develop recommendations 
1398for the core measure and non-core measures to be adopted in the standard quality measure set for 
1399use in: (i) contracts between payers, including the commonwealth and carriers, and health care  66 of 119
1400providers, provider organizations and accountable care organizations, including the designation 
1401of a set of core measures and a set of non-core measures; (ii) assigning tiers to health care 
1402providers in the design of any health plan; (iii) consumer transparency websites and other 
1403methods of providing consumer information; (iv) monitoring system-wide performance; and (v) 
1404reducing provider administrative burdens related to quality measure reporting.
1405 (4) In developing its recommendations for the standard quality measure set, the statewide 
1406advisory committee shall incorporate recognized quality and safety measures including, but not 
1407limited to, measures used by the Centers for Medicare and Medicaid Services, the group 
1408insurance commission, carriers and providers and provider organizations in the commonwealth 
1409and other states, as well as other valid measures of health care provider performance and 
1410outcomes, including patient-reported outcomes and functional status, patient experience, health 
1411disparities and population health. The statewide advisory committee shall consider measures 
1412applicable to primary care 	providers, specialists, hospitals, provider organizations, accountable 
1413care organizations, oral health providers and other types of providers and measures applicable to 
1414different patient populations. 
1415 (5) Not later than January 1 in each even-numbered year, the statewide advisory 
1416committee shall submit to the center its recommendations on the core measures and non-core 
1417measures to be adopted, changed or updated by the center in the standard quality measure set, 
1418along with a report in support of its recommendations.
1419 SECTION 68. Section 15 of said chapter 12C, as so appearing, is hereby amended by 
1420striking out, in line 4, the word “injury” and inserting in place thereof the following word:- harm. 67 of 119
1421 SECTION 69. Said section 15 of said chapter 12C, as so appearing, is hereby further 
1422amended by striking out the definition of “Board” and inserting in place thereof the following 3 
1423definitions:- 
1424 “Agency”, an agency of the executive branch 	of the commonwealth including, but not 
1425limited to, a constitutional or other office, executive office, department, division, bureau, board, 
1426commission or committee thereof, or any authority created by the general court to serve a public 
1427purpose, having either statewide or local jurisdiction. 
1428 “Board”, the patient safety and medical errors reduction board.
1429 “Healthcare-associated infection”, an infection that a patient acquires during the course of 
1430receiving treatment for other conditions within a health care setting.
1431 SECTION 70. Said section 15 of said chapter 12C, as so appearing, is hereby further 
1432amended by inserting after the definition of “Patient safety” the following definition:-
1433 “Patient safety information”, data and information related to patient safety, including 
1434adverse events, incidents, medical errors or health care-associated infections, that is collected or 
1435maintained by agencies.
1436 SECTION 71. Said section 15 of said chapter 12C, as so appearing, is hereby further 
1437amended by striking out subsection (f) and inserting in place thereof the following 3 
1438subsections:-
1439 (f) Notwithstanding any general or special law to the contrary, the Lehman center and 
1440any agency, provider organization, department, division, commission, board, authority or other 
1441public or quasi-public entity in the commonwealth that collects or maintains patient safety  68 of 119
1442information may transmit such information, including personal data as defined in section 1 of 
1443chapter 66A, to each other, and shall transmit such information to the Lehman center upon 
1444request from the Lehman center; provided, however, that transmission of such information shall 
1445be governed by an agreement, which may be an interagency service agreement, between the 
1446party transmitting the information and the Lehman center; provided further, that such agreement 
1447shall provide for any safeguards necessary to protect the privacy and security of the information; 
1448and provided further, that the transmission of such information shall be in compliance with 
1449federal law. 
1450 (g) The Lehman center may adopt rules and regulations necessary to carry out the 
1451purpose of this section. The Lehman center may contract with any federal, state or municipal 
1452entity or other public institution or with any private individual, partnership, firm, corporation, 
1453association or other entity to manage its affairs or carry out the purpose of this section. 
1454 (h) The Lehman center shall report annually to the joint committee on health care 
1455financing regarding the progress made in improving patient safety and medical error reduction. 
1456The Lehman center may seek federal and foundation support to supplement state resources to 
1457carry out the Lehman center’s patient safety and medical error reduction goals.
1458 SECTION 72. Section 16 of said chapter 12C, as so appearing, is hereby amended by 
1459inserting after the word “publish”, in line 1, the following words:- , for the most recently 
1460concluded benchmark cycle, .
1461 SECTION 73. Said section 16 of said chapter 12C, as so appearing, is hereby further 
1462amended by inserting after the word “submitted”, in line 2, the following words:- for that 
1463benchmark cycle . 69 of 119
1464 SECTION 74. Said section 16 of said chapter 12C, as so appearing, is hereby further 
1465amended by striking out, in line 7, the word “benchmark” and inserting in place thereof the 
1466following words:- and affordability benchmarks.
1467 SECTION 75. Said section 16 of said chapter 12C, as so appearing, is hereby further 
1468amended by striking out, in line 8, the words “section 9” and inserting in place thereof the 
1469following words:- sections 9 and 9A.
1470 SECTION 76. Said section 16 of said chapter 12C, as so appearing, is hereby further 
1471amended by striking out, in line 43, the words “and (12)” and inserting in place thereof the 
1472following words:- (12) a standard set of measures of health care affordability in the 
1473commonwealth, including family health care expenditures and an annual index of how such 
1474health care costs compare to the health care affordability benchmark set under section 9A of 
1475chapter 6D; and (13).
1476 SECTION 77. Said chapter 12C of the General Laws is hereby amended by striking out 
1477sections 17 and 18, as so appearing, and inserting in place thereof the following 2 sections:-
1478 Section 17. The attorney general may review and analyze any information submitted to 
1479the center by a provider, provider organization, private equity firm, real estate investment trust, 
1480management services organization, pharmaceutical manufacturing company, pharmacy benefit 
1481manager or payer pursuant to sections 8, 9 and 10 of this chapter, and to the commission under 
1482section 8 of chapter 6D. The attorney general may require that such entities produce documents, 
1483answer interrogatories and provide testimony under oath related to health care costs and cost 
1484trends, factors that contribute to cost growth within the commonwealth’s health care system and 
1485the relationship between provider costs and payer premium rates. The attorney general shall keep  70 of 119
1486confidential all nonpublic information and documents obtained under this section and shall not 
1487disclose the information or documents to any person without the consent of the entity that 
1488produced the information or documents; provided, however, that the attorney general may 
1489disclose such information or documents during (i) the annual hearing conducted under section 8 
1490of chapter 6D, (ii) a rate hearing before the health insurance bureau, or (iii) in a case brought by 
1491the attorney general, if the attorney general believes that such disclosure will promote the health 
1492care cost containment goals of the commonwealth and that the disclosure would be in the public 
1493interest after taking into account any privacy, trade secret or anti-competitive considerations. The 
1494confidential information and documents shall not be public records and shall be exempt from 
1495disclosure under clause Twenty-sixth of section 7 of chapter 4 or section 10 of chapter 66.
1496 Section 18. (a) The center shall perform ongoing analysis of data it receives under this 
1497chapter to identify any health care entity whose: (1) contribution to health care spending levels 
1498and growth, including but not limited to, spending levels and growth as measured by health-
1499status adjusted total medical expense or total medical 	expense, is considered excessive and who 
1500threaten the ability of the state to meet the health care cost growth benchmark established by the 
1501commission under section 9 of chapter 6D; provided further, that the center shall identify cohorts 
1502for similar health care entities and establish differential standards for excessive growth rates 
1503within the health care cost growth benchmark established by the commission under section 9 of 
1504chapter 6D, based on factors which may include, but are not limited to, a health care entity’s 
1505spending, pricing levels and payer mix; or (2) data is not submitted to the center in a proper, 
1506timely or complete manner.
1507 (b) The center shall confidentially provide a list of the health care entities to the 
1508commission such that the commission may pursue further action under section 10 of chapter 6D.  71 of 119
1509Confidential referrals under this section shall not preclude the center from using its authority to 
1510assess penalties for noncompliance under section 11.
1511 SECTION 78. Section 10 of chapter 13 of the General Laws, as so appearing, is hereby 
1512amended by striking out the last paragraph and inserting in place thereof the following 
1513paragraph:-
1514 The board may: (i) adopt, amend and rescind such rules and regulations as it deems 
1515necessary to carry out this chapter subject to the approval of the commissioner of public health; 
1516(ii) make contracts and arrangements for the performance of administrative and similar services 
1517required or appropriate in the performance of the duties of the board; and (iii) adopt and make 
1518public rules of procedure and other regulations not inconsistent with other provisions of the 
1519General Laws. The commissioner of public health shall appoint an executive director and a legal 
1520counsel for the board.
1521 SECTION 79. Said chapter 13 is hereby further amended by striking out section 10A, as 
1522so appearing, and inserting in place thereof the following section:-
1523 Section 10A. The commissioner of public health shall review and approve any rule or 
1524regulation proposed by the board of registration in medicine pursuant to section 10. Such rule or 
1525regulation shall be deemed disapproved unless approved within 60 days of submission to the 
1526commissioner pursuant to said section 10.
1527 SECTION 80. Chapter 26 of the General Laws is hereby amended by striking out section 
15287A, as so appearing, and inserting in place thereof the following section:- 72 of 119
1529 Section 7A. (a) As used in this section, the following words shall, unless the context 
1530clearly requires otherwise, have the following meanings:-
1531 “Bureau”, health insurance bureau. 
1532 “Deputy commissioner”, the deputy commissioner of the health insurance bureau. 
1533 “Health benefit plan”, any individual, general, blanket or group policy of health, accident 
1534and sickness insurance issued by an insurer licensed under chapter 175; an individual or group 
1535hospital service plan issued by a non-profit hospital service corporation under chapter 176A; an 
1536individual or group medical service plan issued by a nonprofit medical service corporation under 
1537chapter 176B; an individual or group health maintenance contract issued by a health maintenance 
1538organization under chapter 176G, and a dental service plan offered by a dental service 
1539corporation under chapter 176E. Health benefit plans shall not include: (i) accident only, credit 
1540only, limited scope vision if offered separately; (ii) hospital indemnity insurance policies that 
1541provide a benefit to be paid to an insured or a dependent, including the spouse of an insured, on 
1542the basis of a hospitalization of the insured or a dependent, that are sold as a supplement and not 
1543as a substitute for a health benefit plan and that meet any requirements set by the commissioner 
1544by regulation; (iii) disability income insurance; (iv) coverage issued as a supplement to liability 
1545insurance; (v) specified disease insurance that is purchased as a supplement and not as a 
1546substitute for a health plan and meets any requirements the commissioner by regulation may set; 
1547(vi) insurance arising out of a workers' compensation law or similar law; (vii) automobile 
1548medical payment insurance; (viii) insurance under which benefits are payable with or without 
1549regard to fault and which is statutorily required to be contained in a liability insurance policy or 
1550equivalent self-insurance; (ix) long-term care if offered separately; (x) coverage supplemental to  73 of 119
1551the coverage provided under 10 U.S.C. 55 if offered as a separate insurance policy; (xi) travel 
1552insurance; or (xii) any policy subject to chapter 176K or any similar policies issued on a group 
1553basis, Medicare Advantage plans or Medicare Prescription drug plans. A health plan issued, 
1554renewed or delivered within or without the commonwealth to an individual who is enrolled in a 
1555qualifying student health insurance program under section 18 of chapter 15A shall not be 
1556considered a health plan for the purposes of this chapter and shall be governed by said chapter 
155715A; provided, however, that travel insurance for the purpose of this chapter is insurance 
1558coverage for personal risks incident to planned travel, including, but not limited to: (A) 
1559interruption or cancellation of trip or event; (B) loss of baggage or personal effects; (C) damages 
1560to accommodations or rental vehicles; or (D) sickness, accident, disability or death occurring 
1561during travel, provided, however, that the health benefits are not offered on a stand-alone basis 
1562and are incidental to other coverages; and provided further, that the term “travel insurance” shall 
1563not include major medical plans, which provide comprehensive medical protection for travelers 
1564with trips lasting 6 months or longer, including for example, those working overseas as ex-patriot 
1565or military personnel being deployed.
1566 “Rate review”, any examination performed by the deputy commissioner of the aggregate 
1567rates of payment pursuant to sections 5, 6 and 10 of chapter 176A; section 4 of chapter 176B; 
1568section 16 of chapter 176G; section 6 of chapter 176J; and section 7 of chapter 176K.
1569 (b) There shall be within the division of insurance a health insurance bureau overseen by 
1570a deputy commissioner, whose duties shall include, but not be limited to, rate review of premium 
1571rates for health benefit plans offered, issued or renewed in the commonwealth, administration of 
1572the division's statutory and regulatory authority for oversight of the small group and individual 
1573health insurance market, oversight of affordable health plans, including coverage for young  74 of 119
1574adults, as well as the dissemination of appropriate information to consumers about health 
1575insurance coverage and access to affordable products. The deputy commissioner shall: (i) protect 
1576the interests of consumers of health insurance; (ii) encourage fair treatment of health care 
1577providers by health insurers; (iii) enhance equity, access, quality and affordability in the health 
1578care system; (iv) guard the solvency of health insurers; (v) work cooperatively with the health 
1579policy commission and the center for health information and analysis to monitor health care 
1580spending; and (vi) consider affordability of health insurance products during rate review.
1581 (c) The deputy commissioner shall develop affordability standards to consider during rate 
1582review; provided, however, that the deputy commissioner’s review of a carrier’s rates shall 
1583adhere to principles of solvency and actuarial soundness. Such standards shall consider factors 
1584including, but not limited to: (i) affordability for consumers, including the totality of costs paid 
1585by consumers of health insurance for covered benefits including, but not limited to, the enrollee’s 
1586share of premium, out-of-pocket maximum amounts, deductibles, copays, coinsurance and other 
1587forms of cost sharing for health insurance coverage; (ii) affordability for purchasers, including 
1588the totality of costs paid by purchasers of health insurance including, but not limited to, premium 
1589costs, actuarial value of coverage for covered benefits and the value delivered on health care 
1590spending in terms of improved quality and cost efficiency; and (iii) the impact of proposed rates 
1591on the commonwealth’s performance against the health care cost growth benchmark established 
1592in section 9 of chapter 6D and the affordability benchmark established in section 9A of said 
1593chapter 6D.
1594 (d) The deputy commissioner shall review data and documents submitted to the division, 
1595including, but not limited to, any materials submitted as part of rate reviews, to examine the 
1596causes of premium rate increases and excessive provider price variation. 75 of 119
1597 (e) The commissioner shall appoint, at a minimum, the following employees to the 
1598bureau: a deputy commissioner, a general counsel, a chief health economist, a chief actuary, a 
1599chief research analyst and a chief examiner. The appointed employees shall devote their full time 
1600to the duties of their offices, shall be exempt from chapters 30 and 31 and shall serve at the 
1601pleasure of the commissioner. The commissioner may appoint and remove additional employees, 
1602including, but not limited to, a first deputy, economists, analysts, examiners, assistant actuaries, 
1603inspectors, clerks and other assistants as the work of the division may require. Such additional 
1604employees shall perform such duties as the commissioner may prescribe.
1605 (f) The commissioner shall make and collect an assessment against the carriers licensed 
1606under chapters 175, 176A, 	176B, 176E, 176F and 176G to pay for the expenses of the bureau. 
1607The assessment shall be at a rate sufficient to produce $1,000,000 annually. In addition to that 
1608amount, the assessment shall include an amount to be credited to the General Fund which shall 
1609be equal to the total amount of funds estimated by the secretary of administration and finance to 
1610be expended from the General Fund for indirect and fringe benefit costs attributable to the 
1611personnel costs of the bureau. The assessment shall be allocated on a fair and reasonable basis 
1612among all carriers licensed under said chapters. The funds produced by the assessments shall be 
1613expended by the bureau, in addition to any other funds which may be appropriated, to assist in 
1614defraying the general operating expenses of the division and may be used to compensate 
1615consultants retained by the bureau. A carrier licensed under said chapters shall pay the amount 
1616assessed against it within 30 days after the date of the notice of assessment from the 
1617commissioner.
1618 (g) Notwithstanding any general or special law to the contrary, carriers offering health 
1619benefit plans, including carriers licensed under chapter 175, 176A, 176B or 176G, shall annually  76 of 119
1620file a summary of negotiated rate increases for their largest providers, by provider group to the 
1621bureau. The deputy commissioner shall confidentially provide such information to the health 
1622policy commission. 
1623 Rates of reimbursement or rate increases submitted for review by the bureau under this 
1624section shall be deemed confidential and exempt from the definition of public records in clause 
1625Twenty-sixth of section 7 of chapter 4 or section 10 of chapter 66. The deputy commissioner 
1626shall adopt regulations to carry out this section.
1627 SECTION 81. Subsection (b) of section 7H½ of chapter 29 of the General Laws, as so 
1628appearing, is hereby amended by striking out the first sentence and inserting in place thereof the 
1629following sentence:- Annually, not later than January 15, the secretary of administration and 
1630finance shall meet with the house and senate committees on ways and means and shall jointly 
1631develop a growth rate of potential gross state product for the calendar year that will begin 2 years 
1632following the calendar year in which the January 15 date occurs, which shall be agreed to by the 
1633secretary and the committees. 
1634 SECTION 82. Section 9-609 of chapter 106 of the General Laws, as so appearing, is 
1635hereby amended by adding the following subsection:-
1636 (d) Notwithstanding subsection (a), in the case of a debtor that is a hospital licensed by 
1637the department of public health under section 51 of chapter 111 and collateral that is a medical 
1638device, a secured party shall send notice to the debtor and the department of public health not 
1639less than 90 days prior to taking possession of the collateral, rendering equipment unusable or 
1640disposing of the collateral on the debtor’s premises pursuant to subsection (a). For the purposes  77 of 119
1641of this subsection, “medical device” shall have the same meaning as that term is defined in 
1642section 1 of chapter 111N.
1643 SECTION 83. Section 1 of chapter 111 of the General Laws, as so appearing, is hereby 
1644amended by inserting after the definition “Nuclear reactor” the following definition:- 
1645 “Party of record”, during the pendency of an application for a determination of need, an 
1646applicant for a determination of need, the attorney general, the center for health information and 
1647analysis, the health policy commission, any government agency with relevant oversight or 
1648licensure authority over the proposed project or components therein or any 10 taxpayers of the 
1649commonwealth organized as a group.
1650 SECTION 84. Section 25A of said chapter 111, as so appearing, is hereby amended by 
1651striking out the first 5 paragraphs.
1652 SECTION 85. Section 25C of said chapter 111, as so appearing, is hereby amended by 
1653striking out subsections (g) to (j), inclusive, and inserting in place thereof the following 4 
1654subsections:-
1655 (g) The department, in making any determination of need, shall: (i) assess both the 
1656applicant and the proposed project; (ii) be guided by the state health plan and focused health 
1657assessments pursuant to section 22 of chapter 6D and the health care resources inventory 
1658pursuant to section 9 of chapter 12C; (iii) encourage appropriate allocation of private and public 
1659health care resources and the development of alternative or substitute methods of delivering 
1660health care services so that adequate health care services will be made reasonably available to 
1661every person within the commonwealth at the lowest 	reasonable aggregate cost; (iv) be guided 
1662by the commonwealth’s cost containment and affordability goals; (v) assess the impacts on the  78 of 119
1663applicant’s patients and on other residents of the commonwealth, including, but not limited to, 
1664considerations of health equity and the workforce of surrounding health care providers; and (vi) 
1665take into account any comments and relevant data from the center for health information and 
1666analysis, the health policy commission, including, but not limited to, any cost and market impact 
1667review report pursuant to subsection (f) of section 13 of chapter 6D, and any other state agency 
1668or entity. The department may impose reasonable terms and conditions on the approval of a 
1669determination of need as the department determines are necessary to achieve the purposes and 
1670intent of this section, including, but not limited to, conditions intended to address health care 
1671disparities and better align a project with community needs. The department may recognize the 
1672special needs and circumstances of projects that: (i) are essential to the conduct of research in 
1673basic biomedical or health 	care delivery areas or to the training of health care personnel; (ii) are 
1674unlikely to result in any increase in the clinical bed capacity or outpatient load capacity of the 
1675facility; and (iii) are unlikely to cause an increase in the total patient care charges of the facility 
1676to the public for health care services, supplies and accommodations, as such charges shall be 
1677defined from time to time in accordance with section 5 of chapter 409 of the acts of 1976. The 
1678department may also recognize the special needs and circumstances of projects that may address 
1679a lack of supply for a specific region, population or service line that has been identified in the 
1680state health plan or focused assessments pursuant to section 22 of chapter 6D.
1681 (h) Applications for such determination shall be filed with the department, together with 
1682other forms and information as shall be prescribed by, or acceptable to, the department. No 
1683provider or provider organization may apply for a notice of determination of need until a 
1684material change notice, if required, has been submitted to the health policy commission under 
1685section 13 of chapter 6D. A duplicate copy of any application together with supporting  79 of 119
1686documentation for such application, shall be a public record and kept on file in the department. 
1687The department may require a public hearing on any application at its discretion or at the request 
1688of the attorney general. The attorney general may intervene in any hearing under this section. A 
1689reasonable fee, established by the department, shall be paid upon the filing of such application; 
1690provided, however, that such fee shall not exceed 0.2 per cent of the capital expenditures, if any, 
1691proposed by the applicant. The department may adapt the information required and fees required 
1692for applications if it determines a project or class of projects may address a lack of supply for a 
1693specific region, population or service line that has been identified in the state health plan or 
1694focused assessments pursuant to section 22 of chapter 6D. The department may also require an 
1695independent cost analysis be conducted, at the expense of the applicant, by an entity selected and 
1696overseen by the department, including, but not limited to, another state agency, to demonstrate 
1697that the application is consistent with the commonwealth's efforts to meet the health care cost 
1698containment goals established by the commission. Such entity may request, and the applicant 
1699may not unreasonably withhold, confidential data and documents necessary to conduct an 
1700independent cost analysis pursuant to such section; provided, however, that any confidential data 
1701and documents so requested shall be provided to the entity conducting the independent cost 
1702analysis, the department, the health policy commission and the attorney general, but shall not be 
1703disclosed to any other person without the consent of the applicant, except in summary form, or 
1704when the department, health policy commission or attorney general determines that such 
1705disclosure should be made in the public interest after taking into account any privacy, trade 
1706secret or anticompetitive considerations; and provided further, that any confidential data and 
1707documents so provided shall not be public records and shall be exempt from disclosure under 
1708clause Twenty-sixth of section 7 of chapter 4 or section 10 of chapter 66. 80 of 119
1709 (i) Except in the case of an emergency situation determined by the department as 
1710requiring immediate action to prevent further damage to the public health or to a health care 
1711facility, the department shall not act upon an application for such determination unless: (i) the 
1712application has been on file with the department for not less than 30 days; (ii) the center for 
1713health information and analysis, the health policy commission, the office of the attorney general, 
1714the state and appropriate regional comprehensive health planning agencies and, in the case of 
1715long-term care facilities only, the department of elder affairs, or in the case of any facility 
1716providing inpatient services for individuals with intellectual or developmentally disabilities, the 
1717departments of mental health or developmental services, respectively, have been provided copies 
1718of such application and supporting documents and given reasonable opportunity to supply 
1719required information and comment on such application; and (iii) a public hearing has been held 
1720on such application when requested by the applicant, the state or appropriate regional 
1721comprehensive health planning agency, any 10 taxpayers of the commonwealth or any other 
1722party of record. If, in any filing period, an individual application is filed that would implicitly 
1723decide any other application filed during such period, the department shall not act only upon an 
1724individual application.
1725 (j) The department shall so approve or disapprove, in whole or in part, each such 
1726application for a determination of need not more than 6 months after filing with the department; 
1727provided, however, that the department may, on not more than 1 occasion, delay the action for up 
1728to 2 months after the applicant has provided information which the department has reasonably 
1729requested during the 8-month period; provided further, that: (i) the period for review of an 
1730application for which an independent cost analysis is conducted pursuant to subsection (h) shall 
1731be stayed until a completed independent cost analysis is received and accepted by the  81 of 119
1732department: (ii) the period of review of an application for which the commission conducts a cost 
1733and market impact review shall be stayed until a final cost and market impact review has been 
1734issued: and (iii) the period of review of an application for which the applicant is subject to a 
1735performance improvement plan pursuant to section 10 of chapter 6D shall be stayed until the 
1736commission determines that the applicant is implementing or has implemented said performance 
1737improvement plan in good faith; and provided further, that the commission may rescind its 
1738determination that the applicant is implementing a performance improvement plan in good faith 
1739at any time prior to successful completion of the performance improvement plan. Applications 
1740remanded to the department by the health facilities appeals board under section 25E shall be 
1741acted upon by the department within the same time limits provided in this section for the 
1742department to approve or disapprove applications for a determination of need. If an application 
1743has not been acted upon by the department within such time limits, the applicant may, within a 
1744reasonable period of time, bring an action in the nature of mandamus in the superior court to 
1745require the department to act upon the application.
1746 SECTION 86. Said section 25C of said chapter 111, as so appearing, is hereby further 
1747amended by adding the following 2 subsections:-
1748 (o) Notwithstanding sections (a) through (d), the department may create a process under 
1749which persons or entities proposing a project that would normally require a determination of 
1750need may apply for a waiver of such requirement. Such waiver shall be granted only in cases in 
1751which the person or entity demonstrates the project will address a lack of supply for a specific 
1752region, population or service line that has been identified in the state health plan or focused 
1753assessments pursuant to section 22 of chapter 6D. The department may require a waiver request 
1754be accompanied by forms and information as shall be prescribed by, or acceptable to, the  82 of 119
1755department. A duplicate copy of any waiver request together with supporting documentation for 
1756such application shall be a public record and kept on file in the department.
1757 (p) A party of record may review an application for determination of need and provide 
1758written comment or specific recommendations for consideration by the department. Whenever a 
1759party of record submits written materials concerning an application for determination of need, 
1760the department shall provide copies of such materials to all other parties of record.
1761 SECTION 87. Section 25F of said chapter 111, as so appearing, is hereby amended by 
1762inserting after the word “care”, in line 7, the following word:- financing. 
1763 SECTION 88. Paragraph (4) of subsection (d) of section 51G of said chapter 111, as so 
1764appearing, is hereby further amended by inserting, after the third sentence, the following 
1765sentence:-
1766 The department may seek an analysis of the impact of the closure from the health policy 
1767commission.
1768 SECTION 89. Said subsection (d) of said section 51G of said chapter 111, as so 
1769appearing, is hereby further amended by adding the following 2 paragraphs:-
1770 (7) No original license shall be granted or renewed, to establish or maintain an acute-care 
1771hospital unless: (i) all documents related to any lease, master lease, sublease, license or any other 
1772agreement for the use, occupancy or utilization of the premises occupied by the acute-care 
1773hospital are disclosed to the department upon application for licensure; and (ii) the department 
1774has reviewed such documentation and determined the applicant is suitable for licensure.  83 of 119
1775 (8) No original license shall be granted, nor renewed, to establish or maintain an acute-
1776care hospital, as defined in section 25B, unless the applicant is in compliance with the reporting 
1777requirements established in sections 8 to 10, inclusive, of chapter 12C.
1778 SECTION 90. Section 51H of said chapter 111, as so appearing, is hereby amended by 
1779striking out the definition of “Facility” and inserting in place thereof the following definition:
1780 “Facility”, a hospital, institution for the care of unwed mothers, clinic providing 
1781ambulatory surgery as defined in section 25B, limited-service clinic licensed pursuant to section 
178251J, office-based surgical center licensed pursuant to section 51M or urgent care center licensed 
1783pursuant to section 51N.
1784 SECTION 91. Said section 51H of said chapter 111, as so appearing, is hereby further 
1785amended by inserting after the definition of “Healthcare-associated infection” the following 
1786definition:-
1787 “Operational impairment event”, any action, or notice of impending action, including a 
1788notice of financial delinquency, concerning the repossession of medical equipment or supplies 
1789necessary for the provision of patient care.
1790 SECTION 92. Subsection (b) of said section 51H of said chapter 111, as so appearing, is 
1791hereby amended by adding the following paragraph:- 
1792 An operational impairment event shall be reported by a facility to the department not later 
1793than 1 calendar day after it occurs. Notwithstanding any general or special law to the contrary, no 
1794contract between a facility and a lessor of medical equipment shall authorize the repossession of 
1795medical equipment or supplies unless the lessor provides a notice of financial delinquency to the  84 of 119
1796department not less than 90 days prior to repossession of any medical equipment or supplies 
1797necessary for the provision of patient care. Any provision of any contract or other document 
1798between a lessor of medical equipment and a facility which does not comply with this paragraph 
1799shall be void.
1800 SECTION 93. Said chapter 111 is hereby further amended by inserting after section 51L 
1801the following 2 sections:-
1802 Section 51M. (a) As used in this section, the following words shall, unless the context 
1803clearly requires otherwise, have the following meanings:- 
1804 “Deep sedation”, a drug-induced depression of consciousness during which: (i) the 
1805patient cannot be easily awakened but responds purposefully following repeated painful 
1806stimulation; (ii) the patient’s ability to maintain independent ventilatory function may be 
1807impaired; (iii) the patient may require assistance in maintaining a patent airway and spontaneous 
1808ventilation may be inadequate; and (iv) the patient’s cardiovascular function is usually 
1809maintained without assistance. 
1810 “General anesthesia”, a drug-induced depression of consciousness during which: (i) the 
1811patient is not able to be awakened, even by painful stimulation; (ii) the patient’s ability to 
1812maintain independent ventilatory function is often impaired; (iii) the patient, in many cases, often 
1813requires assistance in maintaining a patent airway and positive pressure ventilation may be 
1814required because of depressed spontaneous ventilation or drug-induced depression of 
1815neuromuscular function; and (iv) the patient’s cardiovascular function may be impaired.  85 of 119
1816 “Minimal sedation”, a drug-induced state during which: (i) patients respond normally to 
1817verbal commands; (ii) cognitive function and coordination may be impaired; and (iii) ventilatory 
1818and cardiovascular functions are unaffected.
1819 “Minor procedures”, (i) procedures that can be performed safely with a minimum of 
1820discomfort where the likelihood of complications requiring hospitalization is minimal; (ii) 
1821procedures performed with local or topical anesthesia; or (iii) liposuction with removal of less 
1822than 500cc of fat under un-supplemented local anesthesia.
1823 “Moderate sedation”, a drug-induced depression of consciousness during which: (i) the 
1824patient responds purposefully to verbal commands, either alone or accompanied by light tactile 
1825stimulation; (ii) no interventions are required to maintain a patent airway; (iii) spontaneous 
1826ventilation is adequate; and (iv) the patient’s cardiovascular function is usually maintained 
1827without assistance. 
1828 “Office-based surgical center”, an office, group of offices, a facility or any portion 
1829thereof owned, leased or operated by 1 or more practitioners engaged in a solo or group practice, 
1830however organized, whether conducted for profit or not for profit, which is advertised, 
1831announced, established or maintained for the purpose of providing office-based surgical services; 
1832provided, however, that “office-based surgical center” shall not include: (i) a hospital licensed 
1833under section 51 or by the federal government; (ii) an ambulatory surgical center as defined 
1834pursuant to section 25B and licensed under said section 51; or (iii) a surgical center performing 
1835services in accordance with section 12M of chapter 112.
1836 “Office-based surgical services”, an ambulatory surgical or other invasive procedure 
1837requiring: (i) general anesthesia; (ii) moderate sedation; or (iii) deep sedation and any liposuction  86 of 119
1838procedure, excluding minor procedures and procedures requiring minimal sedation, where such 
1839surgical or other invasive procedure or liposuction is performed by a practitioner at an office-
1840based surgical center.
1841 (b) The department shall establish rules, regulations and practice standards for the 
1842licensing of office-based surgical centers. In determining rules, regulations and practice 
1843standards necessary for licensure as an office-based surgical center, the department may, at its 
1844discretion, determine which regulations applicable to 	an ambulatory surgical center, as defined in 
1845section 25B, shall apply to an office-based surgical center. The department shall consult with the 
1846board of registration in medicine prior to promulgating regulations or establishing rules or 
1847practice standards pursuant to this section.
1848 (c) The department shall issue for a term of 2 years and renew for a like term, a license to 
1849maintain an office-based surgical center to an entity or organization that demonstrates to the 
1850department that it is responsible and suitable to maintain such a center. An office-based surgical 
1851center license shall list the specific locations on the premises where surgical services are 
1852provided. In the case of the transfer of ownership of an office-based surgical center, the 
1853application of the new owner for a license, when filed with the department on the date of transfer 
1854of ownership, shall have the effect of a license for a period of 3 months. 
1855 (d) An office-based surgical center license shall be subject to suspension, revocation or 
1856refusal to issue or to renew for cause if, in its reasonable discretion, the department determines 
1857that the issuance of such license would be inconsistent with the best interests of the public health, 
1858welfare or safety. Nothing in this subsection shall limit the authority of the department to require  87 of 119
1859a fee, impose a fine, conduct surveys and investigations or to suspend, revoke or refuse to renew 
1860a license issued pursuant to subsection (c).
1861 (e) Initial application and renewal fees for the license shall be established pursuant to 
1862section 3B of chapter 7.
1863 (f) The department may impose a fine of up to $10,000 on a person or entity that 
1864advertises, announces, establishes or maintains an office-based surgical center without a license 
1865granted by the department. The department may impose a fine of not more than $10,000 on a 
1866licensed office-based surgical center for violations of this section or any rule or regulation 
1867promulgated pursuant to this section. Each day during which a violation continues shall 
1868constitute a separate offense. The department may conduct surveys and investigations to enforce 
1869compliance with this section.
1870 (g) Notwithstanding any general or special law or rule to the contrary, the department 
1871may issue a 1-time provisional license to an applicant for an office-based surgical center licensed 
1872pursuant to this section if such office-based surgical center holds: (i) a current accreditation from 
1873the Accreditation Association for Ambulatory Health Care, American Association for 
1874Accreditation of Ambulatory Surgery Facilities, Inc., or the Joint Commission On Accreditation 
1875of Healthcare Organizations; or (ii) a current certification for participation in either Medicare or 
1876Medicaid. The department may approve such a provisional application upon a finding of 
1877responsibility and suitability and that the office-based surgical center meets all other licensure 
1878requirements as determined by the department. Such provisional license issued to an office-based 
1879surgical center shall not be extended or renewed. 88 of 119
1880 Section 51N. (a) As used in this section, the following words shall have the following 
1881meanings unless the context clearly requires otherwise:- 
1882 “Emergency services”, as defined in section 1 of chapter 6D. 
1883 “Urgent care center”, a clinic owned or operated by an entity that is not corporately 
1884affiliated with a hospital licensed under section 51, however organized, whether conducted for 
1885profit or not for profit, that is advertised, announced, established or maintained for the purpose of 
1886providing urgent care services in an office or a group of offices, or any portion thereof, or an 
1887entity that is advertised, announced, established or maintained under a name that includes the 
1888words “urgent care” or that suggests that urgent care services are provided therein and is not 
1889corporately affiliated with a hospital licensed under 51; provided, however, that an urgent care 
1890center shall not include: (i) a hospital licensed under said section 51 or operated by the federal 
1891government or by the commonwealth; (ii) a clinic licensed under said section 51; (iii) a limited 
1892service clinic licensed under section 51J; or (iv) a community health center receiving a grant 
1893under 42 U.S.C. 254b. 
1894 “Urgent care services”, a model of episodic care for the diagnosis, treatment, 
1895management or monitoring of acute and chronic disease or injury that is: (i) for the treatment of 
1896illness or injury that is immediate in nature but does not require emergency services; (ii) 
1897provided on a walk-in basis without a prior appointment; (iii) available to the general public 
1898during times of the day, weekends or holidays when primary care provider offices are not 
1899customarily open; and (iv) not intended, and should not be used for, preventative or routine 
1900services. 89 of 119
1901 (b) The department shall establish rules, regulations and practice standards for the 
1902licensing of urgent care centers. In determining regulations and practice standards necessary for 
1903licensure as an urgent care center, the department may, at its discretion, determine which 
1904regulations applicable to a clinic licensed under section 51, shall apply to an urgent care center. 
1905 (c) The department shall issue for a term of 2 years and renew for a like term, a license to 
1906maintain an urgent care center to an entity or organization that demonstrates to the department 
1907that it is responsible and suitable to maintain such an urgent care center. In the case of the 
1908transfer of ownership of an urgent care center, the application of the new owner for a license, 
1909when filed with the department on the date of transfer of ownership, shall have the effect of a 
1910license for a period of 3 months. 
1911 (d) An urgent care center license shall be subject to suspension, revocation or refusal to 
1912issue or to renew for cause if, in its reasonable discretion, the department determines that the 
1913issuance of such license would be inconsistent with or opposed to the best interests of the public 
1914health, welfare or safety. Nothing in this subsection shall limit the authority of the department to 
1915require a fee, impose a fine, conduct surveys and investigations or to suspend, revoke or refuse to 
1916renew a license issued pursuant to subsection (c).
1917 (e) Initial application and renewal fees for the license shall be established pursuant to 
1918section 3B of chapter 7.
1919 (f) The department may impose a fine of up to $10,000 on a person or entity that 
1920advertises, announces, establishes or maintains an urgent care center without a license granted by 
1921the department. The department may impose a fine of not more than $10,000 on a licensed 
1922urgent care center for violations of this section or any rule or regulation promulgated pursuant to  90 of 119
1923this section. Each day during which a violation continues shall constitute a separate offense. The 
1924department may conduct surveys and investigations to enforce compliance with this section.
1925 (g) Notwithstanding any general or special law or rule to the contrary, the department 
1926may issue a 1-time provisional license to an applicant for an urgent care center if such urgent 
1927care center holds: (i) a current accreditation from the Accreditation Association for Ambulatory 
1928Health Care, Urgent Care Association of America or the Joint Commission On Accreditation of 
1929Healthcare Organizations; or (ii) a current certification for participation in either Medicare or 
1930Medicaid. The department may approve such provisional application upon a finding of 
1931responsibility and suitability and that the urgent care center meets all other licensure 
1932requirements as determined by the department. Such provisional license issued to an urgent care 
1933center shall not be extended or renewed.  
1934 SECTION 94. Said section 218 of said chapter 111, as so appearing, is hereby further 
1935amended by striking out, in line 28, the words “Maintenance Organizations” and inserting in 
1936place thereof the following word:- Plans.
1937 SECTION 95. Said chapter 111, as so appearing, is hereby further amended by inserting 
1938after section 244 the following section:-
1939 Section 245. (a) Pursuant to section 23 of chapter 6D, a private equity firm shall deposit, 
1940upon submission of a notice of material change pursuant to section 13 of chapter 6D, a bond with 
1941the department of public health.
1942 (b) Until such bond has been deposited, the department of public health shall not issue a 
1943license to such provider or provider organization under this chapter, the department of mental 
1944health shall not issue a license to such provider or provider organization under chapter 19, and  91 of 119
1945any determination of need application submitted under sections 25B to 25G, inclusive, of said 
1946chapter 111 or material change notice submitted under section 13 of chapter 6D shall be deemed 
1947incomplete. Notwithstanding any general or special law to the contrary, if the bond has not been 
1948deposited, but the department of public health would otherwise be eligible to collect the bond, 
1949the department shall be permitted to collect from the private equity firm the amount it would 
1950have been able to collect had the bond been deposited. 
1951 (c) The health policy commission shall determine the amount of the bond, which shall 
1952equal 1 year of the provider or provider organization’s average or estimated operating expenses, 
1953plus the estimated cost of hiring an independent supervisor and reasonable staff to supervise and 
1954facilitate collecting and spending the bond. The private equity firm shall maintain the bond for as 
1955long as it has a financial interest in the provider or provider organization, and for 7 years 
1956thereafter.
1957 (d) The department of public health may collect the bond if the health policy commission 
1958provides the department of public health with notification pursuant to subsection (c) of section 
195923 of chapter 6D, or if the provider or provider organization in which the private equity firm has 
1960or had a financial interest declares bankruptcy. The department of public health, in consultation 
1961with the health policy commission and the center for health information and analysis, shall use 
1962the bond proceeds to support the continued provision of health services to patients served by the 
1963provider or provider organization. Prior to spending the bond, the department of public health 
1964shall seek input from the public, including, but not limited to, providers, provider organizations 
1965and patients in the affected region, regarding how to spend the bond. The department of public 
1966health may, in consultation with the health policy commission and center for health information  92 of 119
1967and analysis, select an independent supervisor and reasonable staff to supervise and facilitate 
1968collecting and spending the bond. 
1969 SECTION 96. Section 1 of chapter 112 of the General Laws, as so appearing, is hereby 
1970amended by inserting after the third paragraph the following paragraph:-
1971 The commissioner of occupational licensure and the commissioner of public health shall 
1972by regulation define the words “good moral character”, establish a standardized assessment of 
1973“good moral character” for applicants for certification or licensure. Each of the boards of 
1974registration and examination under supervision of the commissioner of occupational licensure 
1975and the commissioner of public health shall apply said standard definition and assessment of 
1976“good moral character” for applicants of certification 	or licensure. The commissioners shall hold 
1977at least 1 public hearing seeking input on the standard definition and assessment of “good moral 
1978character” for applicants of certification or licensure. 	In developing the standard definition and 
1979assessment of “good moral character”, the commissioners shall consider factors including, but 
1980not limited to: (i) the nature and gravity of any conduct that would cause concerns about an 
1981applicant’s moral character, including whether the conduct demonstrates a disregard for the 
1982welfare, safety or rights of another or disregard for honesty, integrity or trustworthiness; (ii) the 
1983nature of the job; (iii) the length of time that has passed since the conduct; (iv) the circumstances 
1984surrounding the conduct, including the age of the offender and contributing social conditions and 
1985biases; (v) evidence of rehabilitation, including subsequent work history and character 
1986references; and (vi) racial, ethnic and other inequities in the criminal justice system.
1987 SECTION 97. The 	sixth paragraph of section 2 of said chapter 112, as so appearing, is 
1988hereby amended by striking out the last sentence and inserting in place thereof the following  93 of 119
1989sentence:- The renewal application shall be accompanied by a fee determined under the 
1990aforementioned provision and shall include the physician’s name, license number, home address, 
1991office address, specialties, the principal setting of their practice and whether they are an active or 
1992inactive practitioner. 
1993 SECTION 98. Said chapter 112 is hereby further amended by inserting after section 4 the 
1994following 2 sections:-
1995 Section 4A. (a) For the purposes of this section and section 4B, the following words shall 
1996have the following meanings unless the context clearly requires otherwise:
1997 “Clinician”, a physician, nurse, physician assistant, psychologist or independent clinical 
1998social worker, who is licensed to provide health services and registered in the commonwealth 
1999pursuant to this chapter to provide such services, and any other individual who is licensed to 
2000provide health services and registered in the commonwealth pursuant to this chapter to provide 
2001such services.
2002 “Clinician with independent practice authority”, a physician registered to practice 
2003medicine in the commonwealth or a nurse practitioner, psychiatric nurse mental health clinical 
2004specialist or nurse anesthetist who is registered to practice nursing in the commonwealth and 
2005who has independent practice authority pursuant to sections 80E, 80H and 80J. 
2006 “Health care practice”, a business, regardless of form, through which a clinician with 
2007independent practice authority licensed by the board of registration in medicine or the board of 
2008registration in nursing offers health services; provided, however, that “health care practice” shall 
2009not include any entity that holds a license issued by the department of public health pursuant to 
2010sections 51, 51M, 51N or 52 of chapter 111. 94 of 119
2011 “Management services organization”, a business that provides management or 
2012administrative services to a provider or provider organization for compensation.
2013 “Nurse anesthetist”, an advanced practice registered nurse who is authorized advanced 
2014nursing practice in the commonwealth pursuant to sections 80B and 80H.
2015 “Nurse practitioner”, an advanced practice registered nurse who is authorized in 
2016advanced nursing practice in the commonwealth pursuant to sections 80B and 80E.
2017 “Physician”, a doctor of medicine or doctor of osteopathy who is registered to practice 
2018medicine in the commonwealth pursuant to section 2.
2019 “Provider”, shall have the same definition as in section 1 of chapter 6D.
2020 “Provider organization”, shall have the same definition as in section 1 of chapter 6D; 
2021provided, however, that for the purposes of this section, “provider organization” shall not include 
2022a management services organization.
2023 “Psychiatric nurse mental health clinical specialist”, an advanced practice registered 
2024nurse who is authorized in advanced nursing practice in the commonwealth pursuant to sections 
202580B, 80E and 80J. 
2026 (b) A clinician with independent practice authority may practice medicine or nursing at a 
2027health care practice that is: (i) wholly owned and controlled by 1 or more clinicians with 
2028independent practice authority who hold a certificate of registration that: (1) is issued by the 
2029board of registration in medicine or the board of registration in nursing pursuant to the 
2030requirements of sections 2 and 80B of this chapter; and (2) has not been suspended or revoked; 
2031or (ii) conducted through a business organization, a majority share of which is owned by  95 of 119
2032clinicians with independent practice authority or a provider or provider organization, and which 
2033is formed as: (1) a professional corporation pursuant to chapter 156A; (2) a nonprofit 
2034organization, a nonprofit hospital services corporation organized under chapter 176A or a 
2035nonprofit medical services corporation organized under chapter 176B; (3) a limited liability 
2036company organized under chapter 156C; provided, however, that there are no limited liability 
2037company’s provisions limiting or eliminating the licensee's liability for intentional tort or 
2038negligence; (4) a partnership organized under chapter 108A, including, but not limited to, a 
2039registered limited liability partnership; provided, however, that the partnership has no provisions 
2040limiting or eliminating the licensee's liability for intentional torts or negligence; or (5) an 
2041organization similar to those organizations described in clauses (i) to (iv), inclusive, and 
2042organized under a comparable law of any other jurisdiction within the United States; provided, 
2043however, that a majority share of the organization shall be owned by clinicians with independent 
2044practice authority or a provider organization.
2045 (c) It shall constitute the unauthorized practice of medicine in violation of section 6 for 
2046any person or entity, on their own or in combination with another person or entity, to own a 
2047majority share in a health care practice other than provider or provider organization that is 
2048substantially engaged in delivering health care to patients in the commonwealth or a clinician 
2049with independent practice authority who: (i) holds a certificate of registration that is issued by 
2050the board of registration in medicine or the board of registration in nursing pursuant to the 
2051requirements of sections 2 or 80B and has not been suspended or revoked; and (ii) is 
2052substantially engaged in delivering health care to patients in the commonwealth through the 
2053practice or managing of the health care practice. This section shall not apply to a health care  96 of 119
2054facility or entity that holds a license issued by the department of public health pursuant to 
2055sections 51, 51M, 51N or 52 of chapter 111. 
2056 (d)(1) Nothing in this section shall prohibit a clinician with independent practice 
2057authority from practicing medicine or nursing as an employee of a health care facility or entity 
2058that holds a license issued by the department of public health pursuant to sections 51, 51M, 51N 
2059or 52 of chapter 111. 
2060 (2) Health care facilities or entities that hold a license issued by the department of public 
2061health pursuant to sections 51, 51M, 51N or 52 of chapter 111, providers and provider 
2062organizations shall not, themselves or through a management services organization that the 
2063provider organization fully or partially owns or controls, directly or indirectly interfere with, 
2064control or otherwise direct 	the professional judgment or clinical decisions of clinicians with 
2065independent practice authority who receive compensation, including, but not limited to, as 
2066employees or independent contractors, from the health care facility, provider, provider 
2067organization or an entity that the provider organization fully or partially owns or controls. 
2068Conduct prohibited under this paragraph shall include, but not be limited to, controlling, either 
2069directly or indirectly, through discipline, punishment, threats, adverse employment actions, 
2070coercion, retaliation or excessive pressure, regarding: (i) the amount of time spent with patients, 
2071including the time permitted to triage patients in the emergency department or evaluate admitted 
2072patients; (ii) the time period within which a patient must be discharged; (iii) decisions involving 
2073the patient’s clinical status, including, but not limited to, whether the patient should be kept in 
2074observation status, whether the patient should receive palliative care and where the patient 
2075should be placed upon discharge; (iv) the diagnosis, diagnostic terminology or codes that are 
2076entered into the medical record; or (v) any other conduct the department of public health  97 of 119
2077determines by regulation would interfere with, control or otherwise direct the professional 
2078judgement or clinical decisions of clinicians with independent practice authority. Such health 
2079care facilities or entities shall not limit the range of clinical orders available to clinicians either 
2080directly or by configuring the medical record to prohibit or significantly limit the clinical order 
2081options available. Nondisclosure or non-disparagement agreements regarding subsections (i) 
2082through (v), inclusive, between clinicians with independent practice authority and health care 
2083facilities or entities that hold a license issued by the department of public health pursuant to 
2084sections 51, 51M, 51N or 52 of chapter 111, providers, provider organizations or their corporate 
2085affiliates shall be considered void and unenforceable. If a court of competent jurisdiction finds a 
2086policy, contract or contract provision void and unenforceable pursuant to this section, the court 
2087shall award the plaintiff reasonable attorney’s fees and costs. Nothing in this section shall limit 
2088the ability of any person to bring any action relating to defamation, disclosure of confidential or 
2089proprietary information or trade secrets or similar torts.
2090 (e) All health care practices shall provide written certification that the health care practice 
2091meets the requirements in this section to the board of registration in medicine or the board of 
2092registration in nursing at the time of formation and on a biennial basis thereafter. If a health care 
2093practice’s owners consist of individuals registered solely with the board of registration in 
2094medicine or the board of registration in nursing, the health care practice shall provide the 
2095certification to the applicable board. If the practice’s owners consist of individuals registered 
2096with both boards, the health care practice shall provide the certification to the board of 
2097registration in medicine, which shall transmit a copy to the board of registration in nursing. 
2098Health care practices shall, at the time that such clinicians with independent practice authority 
2099are hired or affiliated with the practice and within 30 days of providing certification to the  98 of 119
2100applicable board pursuant to this section, provide a copy of the most recent certification to all 
2101clinicians with independent practice authority who: (i) engage in providing health services at the 
2102health center practice; and (ii) do not hold any ownership interest in the health center practice. 
2103 (f) Health care practices shall file with the applicable board a registration application 
2104containing such information as the board may reasonably require, including, but not limited to: 
2105(i) the identity of the applicant and of the clinicians with independent practice authority which 
2106constitute the practice; (ii) any management services organization under contract with the health 
2107care practice; (iii) a certified copy of the health care practice’s certificate of organization, if any, 
2108as filed with the secretary of the commonwealth, or any applicable partnership agreement; (iv) 
2109the address of the health care practice; (v) the services provided by the health care practice; and 
2110(vi) any information the board, in consultation with the health policy commission and the center 
2111for health information and analysis, deems relevant for the state health plan and focused 
2112assessments pursuant to section 22 of chapter 6D and the health care resources inventory 
2113pursuant to section 9 of chapter 12C. The application 	shall be accompanied by a fee in an amount 
2114to be determined pursuant to section 3B of chapter 7. All health care practices registered in the 
2115commonwealth shall renew their certificates of registration with the applicable board every 2 
2116years. The board shall share information relevant to the state health plan and focused 
2117assessments pursuant to section 22 of chapter 6D with the commission and information relevant 
2118to the health care resources inventory pursuant to section 9 of section 12C with the center. 
2119 (g) All health care practices with more than 1 clinician with independent practice 
2120authority that constitutes the practice shall designate a clinician with independent practice 
2121authority at the practice to 	serve as health care director; provided, however, that the designated 
2122clinician shall hold a certificate of registration that: (i) is issued by the board of registration in  99 of 119
2123medicine or the board of registration in nursing pursuant to the requirements of sections 2 or 
212480B; and (ii) has not been suspended or revoked. The director shall be responsible for 
2125implementing policies and procedures to ensure compliance with local ordinances and state and 
2126federal laws and regulations governing the practice of medicine or the practice of nursing, 
2127including regulations promulgated and policies established by the applicable board. The board 
2128may impose discipline against the licenses of the director and clinicians with independent 
2129practice authority who own and control the health care practice for failure of the health care 
2130practice to comply with local ordinances and state and federal laws and regulations governing the 
2131practice of medicine or the practice of nursing, including regulations promulgated and policies 
2132established by the applicable board. 
2133 (h) The board of registration in medicine and board of registration in nursing may 
2134promulgate regulations to establish minimum requirements for the conduct of a health care 
2135practice, including, but not limited to: (i) compliance with section 4A; (ii) maintenance and 
2136access to medical records; and (iii) in the event of a planned closure of the health care practice or 
2137an unplanned event that prevents the health care practice from continuing operations, the 
2138development of a continuity plan to: (1) ensure access to medical records, (2) provide notice to 
2139patients; and (3) assist patients with transitioning to a 	new provider. If a practice’s owners 
2140consist of individuals registered solely with the board of registration in medicine or the board of 
2141registration in nursing, the practice shall comply with the applicable board’s regulations. If the 
2142practice’s owners consist of individuals registered with both boards, the practice shall comply 
2143with the regulations issued by the board of registration in medicine. Each board shall consult 
2144with the other when promulgating regulations. 100 of 119
2145 Section 4B. (a) It shall be a violation of this section for a management services 
2146organization to exercise control over clinical decisions. A management services organization, or 
2147any other organization that is not a health care practice, that does any of the following shall be 
2148considered to have control over the clinical decisions of the health care practice: (i) managing, 
2149supervising, evaluating or recommending promotion or discipline of any owner of or clinician 
2150with independent practice authority associated with the health care practice; (ii) negotiating with 
2151third-party payers on behalf of a health care practice without first obtaining informed consent 
2152from the health care practice’s owners; (iii) advertising or otherwise presenting as a health care 
2153practice or provider of health care services; or (iv) performing any other functions that the 
2154department of public health determines, by regulation, confers to a management services 
2155organization or any other entity that is not a health care practice the ability to control the clinical 
2156decisions of the health care practice or its clinicians with independent practice authority.
2157 (b) A health care practice shall maintain ultimate decision-making authority over: (i) 
2158personnel decisions involving clinicians, including, but not limited to, employment status, 
2159compensation, hours or working conditions; (ii) coding or billing decisions; (iii) the selection and 
2160use of property, including, but not limited to, real property, medical equipment or medical 
2161supplies; (iv) the number of patients seen in a given period of time or the amount of time spent 
2162with each patient; (v) the appropriate diagnostic test for medical conditions; (vi) the use of 
2163patient medical records; (vii) referral decisions; or (viii) any other function or decision that the 
2164department of public health determines, by regulation, confers to a management services 
2165organization or any other entity that is not a health care practice the ability to control the clinical 
2166decisions of a health care practice or its clinicians with independent practice authority. 101 of 119
2167 (c) It shall be a violation of this section for a management services organization or any 
2168other entity that is not a health care practice to include in an agreement with any health care 
2169practice provisions that would: (i) restrict the ability of the health care practice or practice owner 
2170to exercise complete, unfettered control and discretion over the finances or capital of the health 
2171care practice, including, but not limited to, restricting the ability to create, buy or sell stock, issue 
2172dividends or sell the health care practice; (ii) restrict the ability of a person who owns stock in 
2173the health care practice to transfer, alienate or otherwise exercise unfettered discretion and 
2174control over their stock; (iii) restrict in any way the ability of the health care practice or 
2175clinicians with independent practice authority associated with the health care practice to provide 
2176health care services in any place, for any entity or in any form otherwise permitted by law; (iv) 
2177restrict the ability of the health care practice to contract with another management services 
2178organization for management or administrative services upon expiration of the current contract; 
2179(v) limit the ability of the health care practice or the practice’s owners, employees or agents to 
2180publicly discuss the business relationship between the health care practice and the management 
2181services organization; provided, however, that this provision shall not limit the ability of any 
2182person to bring any action relating to defamation, disclosure of confidential or proprietary 
2183information or trade secrets or similar torts; (vi) limit access to, take control from or otherwise 
2184obscure from any clinicians providing services in connection with the health care practice, the 
2185price, rate or amount of the charges for their services; (vii) establish, supervise, manage or 
2186otherwise control the health care practice’s officers or directors; or (viii) create any other 
2187situation the department of public health determines, by regulation, could create the possibility of 
2188allowing the management services organization to control the clinical decisions of the health care 
2189practice. 102 of 119
2190 (d) No management services organization shall have any ownership interest in or direct 
2191or indirect control over health care practices for which the management services organization 
2192provides services. No health care practice shall have any ownership interest in or direct or 
2193indirect control over a management services organization unless the management services 
2194organization is fully owned, alone or in combination, by: (i) health care practices substantially 
2195engaged in delivering health care to patients in the commonwealth; (ii) clinicians with 
2196independent practice authority who both: (1) hold a certificate of registration that is issued by the 
2197board of registration in medicine or the board of registration in nursing pursuant to the 
2198requirements of sections 2 and 80B and has not been suspended or revoked; and (2) are 
2199substantially engaged in delivering health care to patients in the commonwealth; or (iii) provider 
2200organizations. For the purposes of this subsection, a de minimis interest in a publicly traded 
2201company held in a mutual fund, index fund or similar financial instrument shall not be 
2202considered an ownership interest.
2203 (e) No person may serve as a director, officer, employee or contractor for both a 
2204management services organization and a health care practice for which the management services 
2205organization provides services; provided, however, that this subsection shall not apply when the 
2206management services organization is fully owned, alone or in combination, by: (i) health care 
2207practices substantially engaged in delivering health care to patients in the commonwealth; (ii) 
2208clinicians with independent practice authority who both: (1) hold a certificate of registration that 
2209is issued by the board of registration in medicine or the board of registration in nursing pursuant 
2210to the requirements of sections 2 and 80B and has not been suspended or revoked; and (2) are 
2211substantially engaged in delivering health care to patients in the commonwealth; or (iii) provider 
2212organizations. 103 of 119
2213 (f) A violation of this section shall constitute the unauthorized practice of medicine in 
2214violation of section 6 or the unauthorized practice of nursing in violation of section 80E, 80H or 
221580J. Any provision of a contract or agreement that has the effect of violating this section shall be 
2216void and unenforceable. If a court of competent jurisdiction finds a policy, contract or contract 
2217provision void and unenforceable pursuant to this section, the court shall award the plaintiff 
2218reasonable attorney’s fees and costs.
2219 (g) The department of public health, in consultation with the health policy commission, 
2220shall promulgate regulations to effectuate the purposes of this section. 
2221 SECTION 99. Section 1 of chapter 175 of the General Laws, as so appearing, is hereby 
2222amended by inserting after the definition of “Foreign company” the following definition:-
2223 “Health insurance company”, a company that engages in the business of health insurance.
2224 SECTION 100. Said section 1 of said chapter 175, as so appearing, is hereby further 
2225amended by inserting after the definition of “Net value of policies” the following definition:-
2226 “Party of record”, for the purpose of a review by the commissioner of a written 
2227agreement for a merger or consolidation of 2 or more health insurance companies, the health 
2228policy commission, the center for health information and analysis, the attorney general, the 
2229center for health information and analysis and any government agency with relevant oversight or 
2230licensure authority over the proposed project or components therein. 
2231 SECTION 101. The fourth paragraph of section 5 of chapter 176A of the General Laws, 
2232as so appearing, is hereby amended by inserting after the fourth sentence the following 
2233sentence:- In determining whether rates of payment under this section are excessive, the  104 of 119
2234commissioner shall consider the affordability for consumers and purchasers of health insurance 
2235products; provided, however, that the commissioner shall not disapprove a carrier’s rates solely 
2236on the basis of the affordability standard. 
2237 SECTION 102. The second paragraph of section 6 of said chapter 176A, as so appearing, 
2238is hereby amended by adding the following sentence:- In determining whether the rates of 
2239payment under a contract are excessive under this section, the commissioner shall consider the 
2240affordability for consumers and purchasers of health insurance products; provided, however, that 
2241the commissioner shall not disapprove a carrier’s rates solely on the basis of the affordability 
2242standard. 
2243 SECTION 103. The third paragraph of section 10 of said chapter 176A, as so appearing, 
2244is hereby amended by inserting after the first sentence the following sentence:- In determining 
2245whether the rates of payment under a contract are excessive under this section, the commissioner 
2246shall consider the affordability for consumers and purchasers of health insurance products; 
2247provided, however, that the commissioner shall not disapprove a carrier’s rates solely on the 
2248basis of the affordability standard. 
2249 SECTION 104. The second paragraph of section 4 of chapter 176B of the General Laws, 
2250as so appearing, is hereby amended by inserting after the second sentence the following 
2251sentence:- In determining whether the rates of payment under an agreement are excessive under 
2252this section, the commissioner shall consider the affordability for consumers and purchasers of 
2253health insurance products; provided, however, that the commissioner shall not disapprove a 
2254carrier’s rates solely on the basis of the affordability standard.  105 of 119
2255 SECTION 105. The first paragraph of section 16 of chapter 176G of the General Laws, 
2256as so appearing, is hereby amended by inserting after the second sentence the following 
2257sentence:- In determining whether the rates of payment under a contract are excessive under this 
2258section, the commissioner shall consider the affordability for consumers and purchasers of health 
2259insurance products; provided, however, that the commissioner shall not disapprove a carrier’s 
2260rates solely on the basis of the affordability standard.
2261 SECTION 106. Subsection (c) of section 6 of chapter 176J of the General Laws, as so 
2262appearing, is hereby amended by inserting after the second sentence the following sentence:- In 
2263determining whether the proposed changes to base rates of payment are excessive under this 
2264section, the commissioner shall consider the affordability for consumers and purchasers of health 
2265insurance products; provided, however, that the commissioner shall not disapprove a carrier’s 
2266proposed changes to base rates solely on the basis of the affordability standard.
2267 SECTION 107. The second paragraph of subsection (g) of section 7 of chapter 176K of 
2268the General Laws, as so appearing, is hereby amended by adding the following sentence:- In 
2269determining whether rates of payment are excessive under this section, the commissioner shall 
2270consider the affordability for consumers and purchasers of health insurance products; provided, 
2271however, that the commissioner shall not disapprove a carrier’s rates solely on the basis of the 
2272affordability standard.
2273 SECTION 108. Section 12 of chapter 176O of the General Laws, as so appearing, is 
2274amended by adding the following subsections:-
2275 (g) For an insured member who is stable on a treatment, service or course of medication 
2276as determined by a health care provider and approved for coverage by a previous carrier or health  106 of 119
2277benefit plan, a carrier or utilization review organization shall not restrict coverage of such 
2278treatment, service or course of medication for at least 90 days upon the insured member’s 
2279enrollment unless the previously approved admission, procedure, treatment, service or course of 
2280medication is not a covered benefit under the insured member’s new plan; provided, however, 
2281that a carrier may condition coverage of continued treatment by a provider under this subsection 
2282upon the provider’s agreeing to accept reimbursement from the carrier at the average in-network 
2283rate and not to impose cost sharing with respect to the insured in an amount that would exceed 
2284the cost sharing imposed if the provider were in network.
2285 (h) Preauthorization approval issued by a carrier for a prescribed maintenance medication 
2286shall be valid for the length of the prescription, as written by the prescriber, up to 1 year. For the 
2287purposes of this section, “maintenance medication” shall mean a prescribed treatment services, 
2288or course of medication intended for chronic disease management.
2289 SECTION 109. The General Laws are hereby amended by inserting after chapter 176X 
2290the following chapter:- 
2291 Chapter 176Y. LICENSING AND REGULATION OF PHARMACY BENEFIT 
2292MANAGERS.
2293 Section 1. As used in this chapter, the following words shall have the following meanings 
2294unless the context clearly requires otherwise:
2295 “Carrier”, an insurer licensed or otherwise authorized to transact accident or health 
2296insurance under chapter 175, a nonprofit hospital service corporation organized under chapter 
2297176A, a nonprofit medical service corporation organized under chapter 176B, a health 
2298maintenance organization organized under chapter 176G or an organization entering into a  107 of 119
2299preferred provider arrangement under chapter 176I; provided, however, that “carrier” shall not 
2300include an employer purchasing coverage or acting on behalf of its employees or the employees 
2301of a subsidiary or affiliated corporation of the employer; and provided further, that unless 
2302otherwise provided, “carrier” shall not include any entity to the extent it offers a policy, 
2303certificate or contract that provides coverage solely for dental care services or vision care 
2304services.
2305 “Center”, the center for health information and analysis established under chapter 12C.
2306 “Commissioner”, the commissioner of insurance.
2307 “Division”, the division of insurance.
2308 “Health benefit plan”, a contract, certificate or agreement entered into, offered or issued 
2309by a carrier to provide, deliver, arrange for, pay for or reimburse any of the costs of health care 
2310services; provided, however, that the commissioner may, by regulation, define other health 
2311coverage as a “health benefit plan” for the purposes of this chapter.
2312 “Pharmacy”, a physical or electronic facility under the direction or supervision of a 
2313registered pharmacist that is authorized to dispense prescription drugs and has entered into a 
2314network contract with a pharmacy benefit manager or a carrier.
2315 “Pharmacy benefit manager”, a person, business or other entity, however organized, that 
2316directly or through a subsidiary provides pharmacy benefit management services for prescription 
2317drugs and devices on behalf of a health benefit plan sponsor, including, but not limited to, a self-
2318insurance plan, labor union or other third-party payer; provided, however, that pharmacy benefit 
2319management services shall include, but not be limited to: (i) the processing and payment of  108 of 119
2320claims for prescription drugs; (ii) the performance of drug utilization review; (iii) the processing 
2321of drug prior authorization requests; (iv) pharmacy contracting; (v) the adjudication of appeals or 
2322grievances related to prescription drug coverage contracts; (vi) formulary administration; (vii) 
2323drug benefit design; (viii) mail and specialty drug pharmacy services; (ix) cost containment; (x) 
2324clinical, safety and adherence programs for pharmacy services; and (xi) management of the cost 
2325of covered prescription drugs; and provided further, that “pharmacy benefit manager” shall not 
2326include a health benefit plan sponsor unless otherwise specified by the division.
2327 Section 2. (a) No person, business or other entity shall establish or operate as a pharmacy 
2328benefit manager without obtaining a license from the division pursuant to this section. A license 
2329may be granted if the division is satisfied that the applicant possesses the necessary organization, 
2330background expertise and financial integrity to supply the services sought to be offered. A 
2331pharmacy benefit manager 	license shall be valid for a period of 3 years and shall be renewable 
2332for additional 3-year periods. The commissioner shall charge application and renewal fees in the 
2333amount of $25,000. In no event may these fees, when combined with the assessment of 
2334pharmacy benefit managers in section 6 of chapter 6D and section 7 of chapter 12C, exceed the 
2335commonwealth’s estimated operating expenses of the pharmacy benefit manager licensure 
2336program.
2337 (b) A license granted pursuant to this section and any rights or interests therein shall not 
2338be transferable.
2339 (c) A person, business or other entity licensed as a pharmacy benefit manager shall 
2340submit data and reporting information to the center according to the standards and methods 
2341specified by the center pursuant to section 10A of chapter 12C. 109 of 119
2342 (d) The division may issue or renew a license pursuant to this section, subject to 
2343restrictions in order to protect the interests of consumers. Such restrictions may include: (i) 
2344limiting the type of services that a license holder may provide; (ii) limiting the activities in which 
2345the license holder may be engaged; or (iii) addressing conflicts of interest between pharmacy 
2346benefit managers and health plan sponsors.
2347 (e) The division shall develop an application for the licensure of pharmacy benefit 
2348managers that shall include, but not be limited to: (i) the name of the applicant or pharmacy 
2349benefit manage; (ii) the address and contact telephone number for the applicant; (iii) the name 
2350and address of the agent of the applicant or pharmacy benefit manager for service of process in 
2351the commonwealth; (iv) the name and address of any person with management or control over 
2352the applicant or pharmacy benefit manager; and (v) any audited financial statements specific to 
2353the applicant or pharmacy benefit manager. An applicant or pharmacy benefit manager shall 
2354inform the division any material change to the information contained in its application, certified 
2355by an officer of the applicant, within 30 days of such 	a change; provided, however, that, once 
2356licensed, a pharmacy benefit manager shall inform the division of any material change to the 
2357information contained in its application, certified by an officer of the pharmacy benefit manager.
2358 (f) The division may suspend, revoke, refuse to issue or renew or place on probation an 
2359application or pharmacy benefit manager license for cause, which shall include, but not be 
2360limited to: (i) the applicant or pharmacy benefit manager engaging in fraudulent activity that is 
2361found by a court of law to be a violation of state or federal law; (ii) the division receiving 
2362consumer complaints that justify an action under this chapter to protect the health, safety and 
2363interests of consumers; (iii) the applicant or pharmacy benefit manager failing to pay an 
2364application or renewal fee for a license; (iv) the applicant or pharmacy benefit manager failing to  110 of 119
2365comply with reporting requirements of the center under section 10A of chapter 12C; or (v) the 
2366applicant or pharmacy benefit manager failing to comply with a requirement of this chapter.
2367 The division shall provide written notice to the applicant or pharmacy benefit manager 
2368and advise in writing of the reason for any suspension, revocation, refusal to issue or renew or 
2369placement on probation of an application or pharmacy benefit manager license. A copy of the 
2370notice shall be forwarded to the center. The applicant or pharmacy benefit manager may make a 
2371written demand upon the division within 30 days of receipt of such notice for a hearing before 
2372the division to determine the reasonableness of the division’s action. The hearing shall be held 
2373pursuant to chapter 30A.
2374 The division shall not suspend or cancel a license unless the division has first afforded 
2375the pharmacy benefit manager an opportunity for a hearing pursuant to said chapter 30A.
2376 (g) If a person, business or other entity performs the functions of a pharmacy benefit 
2377manager in violation of this chapter, the person, business or other entity shall be subject to a fine 
2378of $5,000 per day for each day that the person, business or other entity is found to be in violation. 
2379 (h) A pharmacy benefit manager licensed under this section shall notify a health carrier 
2380client in writing of any activity, policy, practice contract or arrangement of the pharmacy benefit 
2381manager that directly or indirectly presents any conflict of interest to the pharmacy benefit 
2382manager’s relationship with or obligation to the health carrier client.
2383 (i) The division shall promulgate regulations and adopt policies and procedures necessary 
2384to implement this section. 111 of 119
2385 SECTION 110. There shall be a task force to: (i) study primary care access, delivery and 
2386payment in the commonwealth; (ii) develop and issue recommendations to stabilize and 
2387strengthen the primary care system and the primary care workforce; and (iii) increase the 
2388financial investment in and patient access to primary care across the commonwealth. 
2389 (b) The task force shall consist of: the secretary of health and human services or a 
2390designee, who shall serve as co-chair; the executive director of the health policy commission or a 
2391designee, who shall serve as co-chair; the assistant secretary for MassHealth or a designee; the 
2392executive director of the center for health information and analysis or a designee; the 
2393commissioner of insurance or a designee; the chairs of the joint committee on health care 
2394financing or their designees; 1 member from the Massachusetts Academy of Family Physicians, 
2395Inc.; 1 member from the Massachusetts Chapter of the American Academy of Pediatrics; 1 
2396member from the Massachusetts Medical Society with expertise in primary care; 1 member from 
2397the Massachusetts Coalition of Nurse Practitioners, Inc. with expertise in primary care or in 
2398delivering care in a community health center; 1 member from the Massachusetts Association of 
2399Physician Assistants, Inc. with expertise in primary care; 1 member from the National 
2400Association of Social Workers, Inc. – Massachusetts Chapter with expertise in behavioral health 
2401in a primary care setting; 1 member from the Massachusetts League of Community Health 
2402Centers, Inc.; 1 member from the Massachusetts Health and Hospital Association, Inc.; 1 
2403member from the Massachusetts Association of Health Plans, Inc.; 1 member from Blue Cross 
2404and Blue Shield of Massachusetts, Inc.; 1 member from the Association Industries of 
2405Massachusetts; 1 member from the Retailers Association of Massachusetts, Inc.; 1 member from 
2406Health Care For All, Inc.; 1 member from the Massachusetts Chapter of the American College of  112 of 119
2407Physicians; 1 member from the Massachusetts Primary Care Alliance for Patients; and 1 member 
2408from Massachusetts Health Quality Partners, Inc. 
2409 (c) The task force shall develop recommendations to: (i) define primary care services, 
2410codes and providers; (ii) develop a standardized set of data reporting requirements for private 
2411and public health care payers, providers and provider organizations to enable the commonwealth 
2412and private and public health care payers to track payments for primary care services, including, 
2413but not limited to, fee-for-service, prospective payments, value-based payments and grants to 
2414primary care providers, fees levied on a primary care provider by a provider organization or 
2415hospital system of which the primary care provider is affiliated and provider spending on 
2416primary care services; (iii) establish a primary care spending target for private and public health 
2417care payers that reflects the cost to deliver evidence-based, equitable and culturally competent 
2418primary care; (iv) propose payment models to increase private and public reimbursement for 
2419primary care services; (v) assess the impact of health plan design on health equity and patient 
2420access to primary care services; (vi) monitor and track the needs of and service delivery to 
2421residents of the commonwealth; and (vii) create a short-term and long-term workforce 
2422development plan to increase the supply and distribution of and improve working conditions of 
2423primary care clinicians and other primary care workers. The task force may make additional 
2424recommendations and propose legislation necessary to carry out its recommendations. 
2425 (d) The task force shall, in consultation with the center for health information and 
2426analysis, define the data required to satisfy the contents of this section. The center for health 
2427information and analysis shall adopt regulations to require providers and private and public 
2428health care payers to submit data or information necessary for the task force to fulfill its duties 
2429with this section. Any data collected shall be public and available through the Massachusetts  113 of 119
2430Primary Care Dashboard maintained by the center and Massachusetts Health Quality Partners, 
2431Inc. 
2432 (e) Not later than March 15, 2025, the task force shall issue its report of the findings and 
2433recommendations under clauses (i) and (ii) of subsection (c) with the clerks of the senate and the 
2434house of representatives, the senate and house committees on ways and means, the joint 
2435committee on health care financing, the center for health information and analysis, the health 
2436policy commission and the division of insurance. 
2437 (f) Not later than June 15, 2025, the task force shall issue its report of the findings and 
2438recommendations under clause (iii) of subsection (c) with the clerks of the senate and the house 
2439of representatives, the senate and house committees on ways and means, the joint committee on 
2440health care financing, the center for health information and analysis, the health policy 
2441commission and the division of insurance. 
2442 (g) Not later than September 15, 2025, the task force shall issue its report of the findings 
2443and recommendations under clauses (iv) and (v) of subsection (c) with the clerks of the senate 
2444and the house of representatives, the senate and house committees on ways and means, the joint 
2445committee on health care financing, the center for health information and analysis, the health 
2446policy commission and the division of insurance. 
2447 (h) Not later than December 15, 2025, the task force shall issue its report of the findings 
2448and recommendations under clauses (vi) and (vii) of subsection (c) with the clerks of the senate 
2449and the house of representatives, the senate and house committees on ways and means, the joint 
2450committee on health care financing, the center for health information and analysis, the health 
2451policy commission and the division of insurance. 114 of 119
2452 SECTION 111. (a) 	There shall be a task force to study the use of prior authorization for 
2453health care services and its impact on overall costs in the health care system, and delivery of and 
2454access to high quality health care. The task force shall consist of 11 members: the executive 
2455director of the health policy commission or a designee, who shall serve as co-chair; the 
2456commissioner of insurance or a designee, who shall serve as co-chair; the assistant secretary for 
2457MassHealth; the executive director of the group insurance commission; 1 representative from the 
2458Massachusetts Association of Health Plans, Inc.; 1 representative from Blue Cross and Blue 
2459Shield of Massachusetts, Inc.; 1 representative from the Massachusetts Medical Society; 1 
2460representative from the Massachusetts Health and Hospital Association, Inc.; 1 representative 
2461from the Massachusetts Academy of Family Physicians, Inc.; 1 representative from the 
2462Massachusetts League of Community Health Centers, Inc.; 1 representative from Massachusetts 
2463Taxpayers Foundation, Inc.; 1 representative from Associated Industries of Massachusetts; and 1 
2464representative from Health Care For All, Inc.
2465 (b) The task force shall analyze: (i) the services, treatments and medications that require 
2466prior authorization by payers in Massachusetts; (ii) the factors used by payers to determine 
2467whether a service, treatment or medication is appropriate for prior authorization, including 
2468considerations of potential for provider abrasion, adverse impacts on health outcomes, the 
2469availability, and comparative cost and effectiveness of alternative treatment options and risk of 
2470provider overuse of the treatment; (iii) the processes used by payers to obtain prior authorization 
2471for a service, treatment or medication; (iv) the potential for streamlining prior authorization 
2472processes using automation, electronic submissions, gold carding or other means; (v) actuarial 
2473analysis of the impact of prior authorization requirements on the commonwealth’s efforts to meet 
2474the health care cost benchmark established under section 9 of chapter 6D; (vi) any state and  115 of 119
2475federal laws requiring or limiting prior authorization by public or private payers for a service, 
2476treatment or medication; (vii) the feasibility of an easily accessible, publicly available website 
2477with up-to-date information that provides information regarding utilization review requirements 
2478for treatments; (viii) the services that have no or low prior authorization denial rates across 
2479carriers; (ix) administrative barriers preventing active prior authorizations to continue for their 
2480approved duration in instances where an insured individual transitions to a new plan with the 
2481same carrier or to a new carrier; (x) expedited utilization review processes across carriers; and 
2482(xi) barriers to and solutions for providing uniformity in processes or requirements among 
2483different health care segments, including Medicaid, Medicare, fully-insured and self-insured 
2484commercial plans. 
2485 (c) The task force shall develop recommendations regarding: (i) simplifying and 
2486standardizing prior authorization for evidence-based treatments, services or courses of 
2487medication; (ii) improving access to medically necessary covered services for patients; (iii) 
2488reducing the response time from a carrier or utilization review organization for prior 
2489authorization approvals and denials; (iv) reducing administrative barriers and costs related to 
2490prior authorization on health care providers; (v) limiting the recoupment and denial of claims for 
2491medically necessary covered services; (vi) increasing transparency for covered benefits and prior 
2492authorization requirements; (vii) standardizing prior authorization processes, forms and 
2493requirements for use across health insurance carriers; (viii) eliminating prior authorization 
2494requirements for services, treatments, procedures and prescription drugs that have low variation 
2495in utilization across providers or low denial rates; (ix) eliminating prior authorization for or 
2496reducing the prior authorization review process to 24 hours for emergency treatments, services or 
2497courses of medication; (x) ensuring any physician or personnel under the supervision of a  116 of 119
2498physician that is reviewing a prior authorization request for a carrier has the clinical expertise to 
2499treat the medical condition or disease that is the subject of the request; and (xi) removing prior 
2500authorization for certain chronic disease management.
2501 (d) The task force shall develop a report of its findings and recommendations, including 
2502any legislative or regulatory changes necessary to implement its recommendations. The task 
2503force shall file its report with the clerks of the senate and the house of representatives, the senate 
2504and house committees on ways and means and the joint committee on health care financing not 
2505later than July 31, 2025. 
2506 SECTION 112. Notwithstanding any general or special law to the contrary, the division 
2507of insurance shall consider the recommendations issued by the task force established in section 
2508111 in developing and implementing rules, regulations, bulletins or other guidance to simplify 
2509health insurance prior authorization standards and processes.
2510 SECTION 113. (a) 	Notwithstanding any general or special law to the contrary, the 
2511secretary of health and human services shall direct monthly payments to eligible hospitals in the 
2512form of enhanced Medicaid payments, supplemental payments or other appropriate mechanisms. 
2513Each payment made to an eligible hospital shall be allocated in direct proportion to each eligible 
2514hospital’s average monthly Medicaid payments, as determined by the secretary, for inpatient and 
2515outpatient acute hospital services for the preceding year or the most recent year for which data is 
2516available; provided, however, that such enhanced Medicaid payments shall not be used in 
2517subsequent years by the secretary to calculate an eligible hospital’s average monthly payment; 
2518and provided further, that such payments shall not offset existing Medicaid payments for which 
2519an eligible hospital may be qualified to receive. In any fiscal year, the total sum of all payments  117 of 119
2520made to eligible hospitals under this section shall not exceed $45,000,000. Eligible hospitals may 
2521consider expending said payments to strengthen behavioral health supports and services.
2522 (b) The secretary may require as a condition of receiving payment any such reasonable 
2523condition of payment that the secretary determines necessary to ensure the availability, to the 
2524extent possible, of federal financial participation for the payments and the secretary may incur 
2525expenses and the comptroller may certify amounts for payment in anticipation of expected 
2526receipt of federal financial participation for the payments.
2527 (c) The executive office of health and human services may promulgate regulations as 
2528necessary to carry out this section.
2529 (d) For the purposes of this section “eligible hospital” shall mean an acute care hospital 
2530licensed under section 51 of chapter 111 of the General Laws that: (i) has a statewide relative 
2531price less than 0.99, as calculated by the center for health information and analysis according to 
2532data from the most recent available year; (ii) has a public payer mix greater than 63 per cent, as 
2533calculated by the center for health information and analysis according to data from the most 
2534recent available year; and (iii) is not owned by or financially consolidated or corporately 
2535affiliated with a provider organization, as defined by section 1 of chapter 6D of the General 
2536Laws and as reported by the center for health information and analysis in the fiscal year 2022 
2537hospital cost report database: (1) owns or controls 4 or more acute care hospitals licensed under 
2538said section 51 of said chapter 111; or (2) through which the total net assets of all affiliated acute 
2539care hospitals within the provider organization is greater than $800,000,000. 118 of 119
2540 (e) For the purposes of subsection (d), a clinical affiliation with a provider organization, 
2541absent ownership, financial consolidation or corporate affiliation, shall not disqualify an eligible 
2542hospital from payments authorized under this section.
2543 SECTION 114. (a) 	Notwithstanding any general or special law to the contrary, for the 
2544purposes of monitoring and enforcing the health care cost growth benchmark for calendar years 
25452021 to 2025, inclusive, the center for health information and analysis shall apply sections 8, 9, 
254610, 16 and 18 of chapter 12C of the General Laws as those sections are in effect on December 1, 
25472024.
2548 (b) Notwithstanding any general or special law to the contrary, for the purposes of 
2549monitoring and enforcing the health care cost growth benchmark for calendar years 2021 to 
25502025, inclusive, the health policy commission shall apply sections 9 and 10 of chapter 6D of the 
2551General Laws as those sections are in effect on December 1, 2024.
2552 (c) Notwithstanding any general or special law to the contrary, the first benchmark cycle 
2553shall consist of the years 2025 and 2026. The health care cost growth benchmark for that 
2554benchmark cycle shall be the average of the 2025 health care cost growth benchmark that the 
2555health policy commission governing board established in 2024 and the growth rate of potential 
2556gross state product for 2026 established under section 7H½ of chapter 29 of the General Laws. 
2557 (d) Notwithstanding any general or special law to the contrary, not later than April 15, 
25582025, the board shall establish the health care cost growth benchmark pursuant to section 9 of 
2559chapter 6D of the general laws for: (i) the benchmark cycle consisting of the years 2025 and 
25602026; and (ii) the benchmark cycle consisting of the years 2026 and 2027.  119 of 119
2561 (e) Notwithstanding any general or special law to the contrary, on or before January 15, 
25622025, the secretary and house and senate committees on ways and means shall jointly develop 
2563growth rates of potential gross state product pursuant to section 7H½ of chapter 29 of the 
2564General Laws for each of the calendar years of 2026 and 2027.
2565 SECTION 115. Notwithstanding any general or special law, rule or regulation to the 
2566contrary, section 13 of chapter 6D of the General Laws, as amended by this act, shall apply only 
2567to material change notices submitted after the effective date of this act; provided, however, that 
2568said section 13 of said chapter 6D shall apply to material changes that meet all of the following 
2569criteria: (i) the health policy commission received a completed material change notice regarding 
2570the material change on or after March 1, 2024; (ii) the health policy commission has not yet 
2571determined whether to conduct a cost and market impact review in regard to the material change; 
2572and (iii) the health policy commission classifies the material change as involving a provider or 
2573provider organization’s merger or affiliation resulting in an increase in net patient service 
2574revenue of $10,000,000 or 	more. For such material change notices, the health policy commission 
2575shall be permitted to require submission of a new or revised material change form, request 
2576additional documentation and information and take an additional 30 days to conduct its 
2577preliminary review. 
2578 SECTION 116. Notwithstanding any general or special law, rule or regulation to the 
2579contrary, the health policy commission shall submit the first state health plan to the governor and 
2580the general court, as required under section 22 of chapter 6D of the General Laws, on or before 
2581January 1, 2026. 120 of 119
2582 SECTION 117. Notwithstanding any general or special law to the contrary, section 23 of 
2583said chapter 6D shall only 	apply to private equity firms that obtain a financial interest in a 
2584provider or provider organization and to financial actions taken by registered provider 
2585organizations with private equity investment after the effective date of this act.
2586 SECTION 118. Notwithstanding any general or special law, rule or regulation to the 
2587contrary, section 4B of chapter 112 of the General Laws shall apply only to contracts or 
2588agreements between medical practices and management services organizations entered into after 
2589the effective date of this act.
2590 SECTION 119. Section 17 shall take effect on January 1, 2025.
2591 SECTION 120. Section 67 shall take effect on August 1, 2025. 
2592 SECTION 121. All health care practices required to register pursuant to section 4A of 
2593chapter 112 of the General Laws shall register with the board of registration in medicine not later 
2594than January 1, 2026.
2595 SECTION 122. The commissioner of occupational licensure and the commissioner of 
2596public health shall adopt the regulations required under section 96 not later than 6 months after 
2597the effective date of this act.
2598 SECTION 123. The division of insurance shall adopt the rules and regulations required 
2599under section Error! Reference source not found.112 not later than 6 months after the task force 
2600established in section 111 issues its final report and recommendations. 
2601 SECTION 124. Section 113 is hereby repealed. 
2602 SECTION 125. Section 124 shall take effect 2 years from the effective date of this act.