FDA Guides On Generic Development During COVID-19

Q&A Guidance Document Addresses Common Queries From ANDA Applicants

Guidance published by the US FDA in the form of a question-and-answer document addresses questions from ANDA applicants about generic drug development during the COVID-19 pandemic.

COVID Question Mark Coronavirus
The FDA has answered ANDA developers’ questions around COVID-19 • Source: Shutterstock

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