Emergency use authorization or approval for a COVID-19 vaccine before Phase 3 clinical trials are complete could be considered by the U.S. Food and Drug Administratio
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Emergency use authorization or approval for a COVID-19 vaccine before Phase 3 clinical trials are complete could be considered by the U.S. Food and Drug Administratio
The Federal Drug Administration has broadened its emergency use authorization for the anti-viral drug remdesivir to include all hospitalized coronavirus patients, not just those who are so ill they require ventilators or oxygen therapy.