Georgia 2025-2026 Regular Session

Georgia House Bill HB897 Compare Versions

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11 25 LC 57 9000
22 House Bill 897
33 By: Representatives Au of the 50
44 th
55 , Hugley of the 141
66 st
77 , Park of the 107
88 th
99 , Miller of the 62
1010 nd
1111 ,
1212 Frye of the 122
1313 nd
1414 , and others
1515 A BILL TO BE ENTITLED
1616 AN ACT
1717 To amend Chapter 4 of Title 49 of the Official Code of Georgia Annotated, relating to public
1818 1
1919 assistance, so as to make insulin accessible to individuals who are in urgent need of a2
2020 short-term affordable insulin supply; to provide for a short title; to provide for definitions;3
2121 to require a pharmacy to dispense a 30 day supply of insulin to an eligible individual through4
2222 the Urgent Insulin Safety Net Program; to allow a pharmacy to collect a copayment for5
2323 insulin dispensed through such program; to provide for a pharmacy to submit a claim for6
2424 payment or a replacement supply after dispensing insulin through such program; to require7
2525 a manufacturer to reimburse or resupply a pharmacy dispensing insulin through such8
2626 program; to provide for a pharmacy to dispense one additional short-term affordable urgent9
2727 insulin supply under certain conditions; to require the Department of Community Health to10
2828 develop an application form, an information sheet, and satisfaction surveys regarding such11
2929 program; to require a manufacturer of insulin to establish procedures to make insulin12
3030 available under such program; to provide for enforcement, penalties, and appellate13
3131 procedures; to provide for reporting; to provide for related matters; to provide for an effective14
3232 date; to repeal conflicting laws; and for other purposes.15
3333 BE IT ENACTED BY THE GENERAL ASSEMBLY OF GEORGIA:16
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3636 SECTION 1.
3737 17
3838 Chapter 4 of Title 49 of the Official Code of Georgia Annotated, relating to public assistance,18
3939 is amended by adding a new article to read as follows:19
4040 "ARTICLE 10
4141 20
4242 49-4-200.21
4343 This article shall be known and may be cited as the 'Urgent Insulin Safety Net Program22
4444 Act.'23
4545 49-4-201.24
4646 As used in this article, the term:25
4747 (1) 'Board' means the State Board of Pharmacy.26
4848 (2) 'Department' means the Department of Community Health.27
4949 (3) 'Eligible individual' means an individual qualified for assistance under the program28
5050 as provided in Code Section 49-4-204.29
5151 (4) 'Insulin' means various types of insulin analogs and insulin-like medications,30
5252 regardless of activation period or whether the solution is mixed before or after31
5353 dispensation. An insulin product is exempt from the provisions of this article if the32
5454 wholesale acquisition cost of the insulin is $8.00 or less per milliliter or applicable33
5555 National Council for Prescription Drug Plan billing unit for the entire assessment time34
5656 period, adjusted annually based on the Consumer Price Index.35
5757 (5) 'Manufacturer' means a manufacturer engaged in the production of insulin that is36
5858 self-administered on an outpatient basis. Such term shall not include a manufacturer with37
5959 an annual gross revenue of $2 million or less from insulin sales in this state.38
6060 (6) 'Pharmacy' shall have the same meaning as provided in Code Section 26-4-5.39
6161 (7) 'Program' means the Urgent Insulin Safety Net Program as provided for in this article.40
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6464 (8) 'Proper identification' means any document issued by a governmental agency41
6565 containing a description of the individual, such individual's photograph, or both, and42
6666 giving such individual's date of birth and includes, without being limited to, a passport,43
6767 military identification card, driver's license, or an identification card authorized under44
6868 Code Sections 40-5-100 through 40-5-104. Proper identification shall not include a birth45
6969 certificate.46
7070 (9) 'Urgent need of insulin' means having readily available for use less than a seven-day47
7171 supply of insulin and in need of insulin in order to avoid the likelihood of suffering48
7272 significant health consequences.49
7373 49-4-202.50
7474 (a) Upon receipt of a completed, signed, and dated application form, as provided for in51
7575 Code Section 49-4-204, proof of proper identification, and a copy of a current valid insulin52
7676 prescription, a pharmacy shall dispense one 30 day supply of insulin to an eligible53
7777 individual in urgent need of insulin; provided, however, that a pharmacy may dispense one54
7878 additional 30 day supply of insulin within a 12 month period to an eligible individual as55
7979 provided in Code Section 49-4-203.56
8080 (b) The pharmacy may collect a copayment from the individual to whom insulin was57
8181 dispensed through the program to cover such pharmacy's costs of processing and58
8282 dispensing insulin as part of the program in an amount not to exceed $35.00 for the 30 day59
8383 supply of insulin dispensed.60
8484 (c) The pharmacy shall notify the healthcare provider who issued the insulin prescription61
8585 for the eligible individual no later than 72 hours after the insulin is dispensed.62
8686 (d) The pharmacy shall submit to the manufacturer of the dispensed insulin product or to63
8787 the manufacturer's vendor a claim for payment that conforms with the National Council for64
8888 Prescription Drug Program standards for electronic claims processing. The manufacturer65
8989 shall timely reimburse the pharmacy in an amount that covers the pharmacy's acquisition66
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9292 cost for the insulin and shall timely send the pharmacy a replacement supply of the same67
9393 insulin dispensed under the program.68
9494 (e) When the pharmacy dispenses the insulin to the eligible individual, the pharmacy shall69
9595 also provide an information sheet and a survey, as provided for in Code Sections 49-4-20570
9696 and 49-4-206, respectively.71
9797 (f) The pharmacy shall retain a copy of submitted applications for reporting and auditing72
9898 purposes.73
9999 49-4-203.74
100100 (a) A pharmacy shall dispense one additional 30 day supply of insulin to an eligible75
101101 individual in urgent need of insulin within a 12 month period if such individual has applied76
102102 for medical assistance, Georgia Medicaid, or PeachCare for Kids, and has not been77
103103 determined eligible or has been determined eligible and coverage has not become effective.78
104104 (b) To access one additional 30 day supply of insulin, such eligible individual shall attest79
105105 to the pharmacy that the individual meets the requirements of subsection (a) of this Code80
106106 section and shall be in compliance with the requirements provided in Code81
107107 Section 49-4-204.82
108108 49-4-204.83
109109 (a) To be deemed eligible for services under this article, an individual shall attest on an84
110110 application form as provided for in subsection (b) of this Code section that the individual:85
111111 (1) Is a resident of this state;86
112112 (2) Is not enrolled in any medical assistance or other health coverage or prescription drug87
113113 coverage program that limits such enrollee's total amount of cost-sharing for a 30 day88
114114 supply of insulin, including copayments, deductibles, or coinsurance, to $75.00 or less,89
115115 regardless of the type or amount of insulin prescribed;90
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118118 (3) Has not received insulin through the program within the previous 12 months, except91
119119 as provided in Code Section 49-4-203; and92
120120 (4) Has an urgent need of insulin.93
121121 (b) The department shall develop and make available on its website an application form94
122122 for the program.95
123123 49-4-205.96
124124 (a) The department, in coordination with the board, shall develop an information sheet that97
125125 shall include, but shall not be limited to:98
126126 (1) A description of the program, including how to access it;99
127127 (2) Information on applying for medical assistance;100
128128 (3) Information on applying for a qualified health benefit plan offered through the101
129129 exchange as defined in Code Section 33-23-201; and102
130130 (4) Information on accessing healthcare providers who participate in prescription drug103
131131 discount programs, including providers who are authorized to participate in the 340B104
132132 program under section 340B of the federal Public Health Service Act, 42 U.S.C.105
133133 Section 256b, as amended.106
134134 (b) The department shall post the information sheet provided for in subsection (a) of this107
135135 Code section on its website.108
136136 49-4-206.109
137137 (a) The department, in coordination with the board, shall develop a survey to assess an110
138138 eligible individual's satisfaction with the program, including:111
139139 (1) Adequacy of information available and provided to individuals;112
140140 (2) Accessibility to insulin; and113
141141 (3) Individual's ability to access affordable insulin.114
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144144 (b) The department, in coordination with the board, shall develop a survey to assess a115
145145 pharmacy's satisfaction with the program, including:116
146146 (1) Timeliness of reimbursement from the manufacturers for insulin dispensed through117
147147 the program;118
148148 (2) Ease in submitting claims and insulin product orders to the manufacturers; and119
149149 (3) Timeliness of receiving insulin replacement orders from the manufacturers.120
150150 (c) The department shall post the surveys provided for in subsections (a) and (b) of this121
151151 Code section on its website.122
152152 49-4-207.123
153153 Each manufacturer shall:124
154154 (1) Establish procedures to make insulin available in accordance with this article through125
155155 pharmacies to eligible individuals who are in urgent need of insulin;126
156156 (2) Establish a hotline to provide information on the program and shall list on its website127
157157 information about the program; and128
158158 (3) Provide for dedicated personnel to promptly respond to individuals, pharmacies, and129
159159 healthcare providers and the department.130
160160 49-4-208.131
161161 (a) Any person who by means of a false statement, failure to disclose information, or132
162162 impersonation, or by other fraudulent device, obtains or attempts to obtain any assistance,133
163163 benefit, or payment under this article to which such person is not entitled shall be guilty of134
164164 a misdemeanor; provided, however, that if the value of the assistance so obtained exceeds135
165165 $1,500.00, such person shall be guilty of a felony.136
166166 (b)(1) If a manufacturer fails to comply with the provisions of this article, the department137
167167 may assess an administrative penalty of $200,000.00 per month of such noncompliance.138
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170170 (2) Such penalty shall increase to $400,000.00 per month if the manufacturer continues139
171171 to be in noncompliance after six months and shall increase to $600,000.00 per month if140
172172 the manufacturer continues to be in noncompliance after one year.141
173173 (3) The penalty shall remain at $600,000.00 per month for as long as the manufacturer142
174174 continues in noncompliance.143
175175 (c) An individual or entity that is aggrieved by the action of the department pursuant to144
176176 subsection (a) or (b) of this Code section shall be entitled to a hearing conducted in145
177177 accordance with Chapter 13 of Title 50, the 'Georgia Administrative Procedure Act.'146
178178 49-4-209.147
179179 (a) By July 1, 2026, and every July 1 thereafter, each manufacturer shall report to the148
180180 department the following information for the preceding calendar year:149
181181 (1) The number of Georgia residents who accessed and received insulin through the150
182182 program;151
183183 (2) The total value of the insulin, determined by the wholesale acquisition cost of the152
184184 insulin, provided by the manufacturer for the program;153
185185 (3) The adequacy and timeliness of the manufacturer in responding to a pharmacy154
186186 requesting reimbursement or resupply of insulin dispensed through the program;155
187187 (4) Any administrative penalties assessed under Code Section 49-4-208; and156
188188 (5) Any additional information deemed necessary by the department.157
189189 (b) By July 1, 2026, and every July 1 thereafter, a pharmacy that received any applications158
190190 for the program shall report to the department the following information for the preceding159
191191 calendar year:160
192192 (1) The number of applications for an urgent insulin supply received and the number of161
193193 applications for additional urgent insulin supply received;162
194194 (2) The reasons for determinations of ineligibility;163
195195 (3) The amount of insulin dispensed through the program;164
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198198 (4) The average and total amount of copayment collected from individuals;165
199199 (5) The timeliness of manufacturers' responses to requests for payment and re-supply of166
200200 insulin; and167
201201 (6) Any additional information deemed necessary by the department.168
202202 (c) By August 15, 2027, and every August 15 thereafter, the department shall submit to169
203203 the General Assembly a report regarding the implementation of the program under this170
204204 article. Such report shall include the following information for the preceding year:171
205205 (1) The data collected under subsections (a) and (b) of this Code section;172
206206 (2) The results of the satisfaction surveys provided for in Code Section 49-4-206; and173
207207 (3) Any additional information deemed necessary by the department to assess the174
208208 effectiveness of the implementation of the program."175
209209 SECTION 2.176
210210 This Act shall become effective July 1, 2025. 177
211211 SECTION 3.178
212212 All laws and parts of laws in conflict with this Act are repealed.179
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