Oklahoma 2025 Regular Session

Oklahoma Senate Bill SB927 Compare Versions

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2-SB927 HFLR Page 1
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28-HOUSE OF REPRESENTATIVES - FLOOR VERSION
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30-STATE OF OKLAHOMA
31-
32-1st Session of the 60th Legislature (2025)
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3428 ENGROSSED SENATE
3529 BILL NO. 927 By: Hicks of the Senate
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3731 and
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3933 Munson of the House
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4438 An Act relating to the state Medicaid program;
4539 amending 63 O.S. 2021, Section 5030.1, which relates
4640 to the Medicaid Drug Utilization Review Board;
4741 modifying appointmen t procedure for certain members;
4842 updating statutory language; and providing an
4943 effective date.
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5650 BE IT ENACTED BY THE PEOPLE OF THE STATE OF OKLAHOMA:
5751 SECTION 1. AMENDATORY 63 O.S. 2021, Section 5030.1, is
5852 amended to read as f ollows:
5953 Section 5030.1. A. There is hereby created within the Oklahoma
6054 Health Care Authority the Medicaid Drug Utilization Review Board,
6155 which shall be responsible for the development, implementation and
6256 assessment of retrospective and prospective drug u tilization
6357 programs under the direction of the Authority.
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58+B. The Medicaid Drug Utilization Re view Board shall consist of
59+ten (10) members appointed by the administrator of the Authority as
60+follows:
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90-B. The Medicaid Drug Utilization Review Board shall consist of
91-ten (10) members appointed by the administrator of the Authority as
92-follows:
9387 1. Four physicians, licensed and actively engaged in the
9488 practice of medicine or osteopathic medicine in this state, of
9589 which:
9690 a. three shall be physicians , each of whom is chosen from
9791 a list of not less than six three names submitted by
9892 the Oklahoma State Medical Association, and
9993 b. one shall be a physician ch osen from a list of not
10094 less than two names submitted by the Oklahoma
10195 Osteopathic Association;
10296 2. Four licensed pharmacists actively engaged in the practice
10397 of pharmacy, chosen from a list of not less than six names submitted
10498 by the Oklahoma Pharmaceutical Pharmacists Association;
10599 3. One person representing the lay community, who shall not be
106100 a physician or a pharmacist, but shall be a health care professional
107101 with recognized knowledge and expertise in at least one of the
108102 following:
109103 a. clinically appropriate prescribing of covered
110104 outpatient drugs,
111105 b. clinically appropriate dispensing and monitori ng of
112106 covered outpatient drugs,
113107 c. drug use review, evaluation and intervention, and
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108+d. medical quality assurance; and
109+4. One person representing the pharmaceuti cal industry who is a
110+resident of the State of Oklahoma this state, chosen from a list of
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140-d. medical quality assurance; and
141-4. One person representing the pharmaceuti cal industry who is a
142-resident of the State of Oklahoma this state, chosen from a list of
143137 not less than two names submitted by the Pharmaceutical Research and
144138 Manufacturers of America. The member representing the
145139 pharmaceutical industry shall be prohibite d from voting on action
146140 items involving drugs or classes of drugs.
147141 C. Members shall serve ter ms of three (3) years, except that
148142 one physician, one pharmacist and the lay representative shall each
149143 be initially appointed for two -year terms in order to stagg er the
150144 terms. In making the appointments, the administrator shall provide,
151145 to the extent possible, for geographic balance in the representation
152146 on the Medicaid Drug Utilization Review Board. Members may be
153147 reappointed for a period not to exceed three thr ee-year terms and
154148 one partial term. Vacancies on the Medicaid Drug Utilization Review
155149 Board shall be filled for the balance of the unexpired term from new
156150 lists submitted by the entity originally submitting the list for the
157151 position vacated.
158152 D. The Medicaid Drug Utilization Review Board shall elect from
159153 among its members a chair and a vice-chair vice chair who shall
160154 serve one-year terms, provided they may succeed themselves.
161155 E. The proceedings of all meetings of the Medicaid Drug
162156 Utilization Review Board shall comply with the provisions of the
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157+Oklahoma Open Meeting Act and shall be subject to the provisions of
158+the Administrative Procedures Act.
159+F. The Medicaid Drug Utilization Review Board may advise and
160+make recommendations to the Authority regarding ex isting, proposed
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189-Oklahoma Open Meeting Act and shall be subject to the provisions of
190-the Administrative Procedures Act.
191-F. The Medicaid Drug Utilization Review Board may advise and
192-make recommendations to the Authority regarding ex isting, proposed
193187 and emergency rules governing retrospective and prospective drug
194188 utilization programs. The Oklahoma Health Care Authority Board
195189 shall promulgate rules pursuant to the provisions of the
196190 Administrative Procedures Act for implementation of t he provisions
197191 of this section.
198192 SECTION 2. This act shall become effective Nov ember 1, 2025.
193+Passed the Senate the 17th day of March, 2025.
199194
200-COMMITTEE REPORT BY: COMMITTEE ON HEALTH AND HUMAN SERVICES, dated
201-04/16/2025 – DO PASS.
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197+ Presiding Officer of the Senate
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200+Passed the House of Representatives the ____ day of _________ _,
201+2025.
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205+ Presiding Officer of the House
206+ of Representatives
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