It’s official: The Food and Drug Administration has granted emergency use authorization to the
COVID-19 vaccine developed by Pfizer Inc. and its partner BioNTech. The decision was announced Friday night after the White House put pressure on the agency’s chief to make the call by the end of the day.
Emergency use authorization of the two-dose vaccine opens a new chapter in the fight against the deadly disease that scientists, health officials and a beleaguered public all hope will mark the beginning of the pandemic’s end. The first immunizations could begin in a matter of days.
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