FDA Advisory Panel Recommends Moderna COVID-19 Vaccine for EUA

Today, a U.S. Food & Drug Administration (FDA) advisory panel voted (20 in favor, one abstention) to recommend the Moderna COVID-19 vaccine for Emergency Use Authorization (EUA), citing that the benefits of the vaccine outweighed its risks. It is anticipated that the FDA will issue an EUA for the Moderna vaccine tomorrow. This EUA would clear the way for nearly 6 million more vaccine doses to be shipped as early as this weekend. Learn more.


Topics: Vaccine

Written by Argentum

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