Manufacturers of up to 10 high-cost treatments including cell and gene therapies could be required to provide data to Medicaid on pricing, clinical benefit and the cost of production in an annual audit as part of an effort by the federal government to provide states with more tools to negotiate price concessions.
The Centers for Medicare and Medicaid Services described the audit policy in a proposed rule released on 23 May. The proposal also addresses several other policies related to the...
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