Pfizer and Biontech to Submit Emergency Use Authorization Request Yesterday to the U.S. FDA for COVID-19 Vaccine ...Middle East

New York & Mainz, Germany–(BUSINESS WIRE)– Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) announced they will submit a request today to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of their mRNA vaccine candidate, BNT162b2 against SARS-CoV-2, which will potentially enable use of the vaccine in high-risk populations in the U.S. by the middle to end of December 2020. This press release features multimedia. View the full release here: https://www.businesswire.com/news/home/20201120005370/en/ In addition to today’s submission to the FDA, the companies have already initiated rolling submissions across the globe including in Australia, Canada, Europe,

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Pfizer and Biontech to Submit Emergency Use Authorization Request Yesterday to the U.S. FDA for COVID-19 Vaccine ...Middle East

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