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COVID-19 vaccines: Dive deep on emergency use authorization

Amid widespread vaccine hesitancy that could delay efforts to achieve the herd immunity required to end the COVID-19 pandemic, the top official from the Food and Drug Administration’s Center for Biologics Evaluation and Research—Peter Marks, MD, PhD—joined the AMA’s president for an in-depth webinar to answer physicians’ questions and explain how emergency use authorization (EUA) fits into the coronavirus vaccine-approval process.

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