Abuses of FDA regulatory procedures - the case of Suboxone

New England Journal of Medicine

8 January 2020 - The manufacturer of brand-name buprenorphine products exploited various FDA regulatory procedures to impede market entry of generic competitors and to maintain high prices. 

This case provides an example of the kinds of abuses that are common in prescription-drug markets.

Read New England Journal of Medicine Perspective

Michael Wonder

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Michael Wonder

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Medicine , US , Regulation , Safety