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COVID-19: FDA Warning Letters Address Fraudulent Products and Failures to Meet EUA Requirements

Date: 12 November 2020

In this week’s episode, Kenneth Kennedy discusses FDA’s ongoing focus on the issuance of warning letters to firms marketing fraudulent COVID-19 products, and to manufacturers who have failed to meet certain requirements under applicable FDA Emergency Use Authorizations (EUAs), as well as what manufacturers and health care providers alike can learn from this trend.

Kenneth M. Kennedy
Kenneth M. Kennedy
Research Triangle Park
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