‘Normalization’ of Emergency Use Authorizations Concerns Health Experts

‘Normalization’ of Emergency Use Authorizations Concerns Health Experts
Medical syringes with the FDA logo displayed in the background in Krakow, Poland, on Dec. 2, 2021. Jakub Porzycki/NurPhoto via Getty Images
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The Food and Drug Administration (FDA) has approved an unprecedented number of emergency use authorizations (EUAs) for drugs, tests, and medical devices since the beginning of the pandemic.

Between March 2020 and June 2021, more than 600 EUAs were authorized, according to Fortune.
Marina Zhang
Marina Zhang
Author
Marina Zhang is a health reporter for The Epoch Times. She covers both health news and in-depth features on emerging health issues. Marina holds a bachelor's degree in biomedicine from the University of Melbourne. Contact her at [email protected].
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