1. The Authority shall, by regulation, set forth the duties of the Board, which must include, without limitation: (a) Identifying the prescription drugs which should be included on the list of preferred prescription drugs developed by the Authority pursuant to NRS 422.4025 , which must include, without limitation, any prescription drug required by the Centers for Medicare and Medicaid Services of the United States Department of Health and Human Services to be covered by the Medicaid program and any other prescription drug deemed essential by the Board; (b) Identifying the prescription drugs which should be excluded from any restrictions that are imposed by the Medicaid program on drugs that are on the list of preferred prescription drugs; (c) Identifying classes of therapeutic prescription drugs for its review and performing a clinical analysis of each drug included in each class that is identified for review; and (d) Reviewing at least annually all classes of therapeutic prescription drugs on the list of preferred prescription drugs developed by the Authority pursuant to NRS 422.4025 . 2. The Authority shall, by regulation, require the Board to: (a) Base its decisions on evidence of clinical efficacy, safety and outcomes for patients and, if the difference between the clinical efficacy, safety and outcomes for two or more drugs is not clinically significant, cost; (b) Review new pharmaceutical products in as expeditious a manner as possible; and (c) Consider new clinical evidence supporting the inclusion of an existing pharmaceutical product on the list of preferred prescription drugs developed by the Authority and new clinical evidence supporting the exclusion of an existing pharmaceutical product from any restrictions that are imposed by the Medicaid program on drugs that are on the list of preferred prescription drugs in as expeditious a manner as possible. 3. The Authority shall, by regulation, authorize the Board to: (a) In carrying out its duties, exercise clinical judgment and analyze peer review articles, published studies, and other medical and scientific information; and (b) Establish subcommittees to analyze specific issues that arise as the Board carries out its duties. 4. The Board may close any portion of a meeting during which it considers the cost of prescription drugs.
‹ Prev All Nevada sections Next ›
Lexace provides legal information, not legal advice, and no attorney–client relationship is created. Statute text is provided for general information and may not reflect the most recent amendments; verify against the official state code.