Buprenorphine Waiver Sheds Little Light On FDA Decision-Making Process

But the agency appeared willing to consider a waiver because the innovator and generic sponsors could not reach agreement on a shared REMS.

FDA’s decision to allow separate Risk Evaluation and Mitigation Strategies for branded buprenorphine transmucosal products and their generic equivalents has shed little light on how it will apply the statutory criteria for waiving the single shared system requirement.

Nevertheless, the agency’s action suggests it will consider a waiver when the innovator and generic sponsors are unable to agree...

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