FDA Expedites ANDA Postapproval Manufacturing Changes

Acceleration Necessary Due To COVID-19 Impacts

Generic drugs program has approved almost 300 manufacturing changes to help shore up the supply chain, with some prior approval supplements being downgraded to ‘changes being effected’ supplements, FDA officials said at GDUFA III kick-off meeting.

To do list conceptual
Non-industry stakeholders shared their GDUFA III 'to do' list with FDA and generic drug companies • Source: Shutterstock

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