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Business · 27/05/2021

FDA Issues Emergency Use Authorizations for COVID-19 Biological Products

The US Food and Drug Administration (FDA) has granted two Emergency Use Authorizations (EUAs) for biological products to combat COVID-19, following a public health emergency declaration by the Secretary of Health and Human Services in February 2020.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →
Related company profile: Eli Lilly and CompanyOpen profile →Explore businesses on Business Maps →

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