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FDA authorizes Moderna COVID-19 vaccine for emergency use By Matthew Perrone and Lauran Neergaard Published  FDA advisory committee votes to recommend emergency use of Moderna COVID-19 vaccine A key advisory committee to the FDA on Thursday voted to recommend the approval of Moderna’s COVID-19 vaccine for emergency use, one of the final hurdles before FDA authorization. WASHINGTON - The U.S. Food and Drug Administration authorized Moderna’s coronavirus vaccine for emergency use on Friday, the second vaccine to be approved by U.S. regulators to prevent severe COVID-19 illness. FDA Commissioner Stephen M. Hahn, called the approval another crucial step in the fight against this global pandemic.

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