Moderna Applies For Emergency FDA Authorization After Successful Vaccine Trials
Moderna is the second company in the U.S. to release its full trial results and apply for emergency use authorization.
Ask Dr. Nandi: Moderna requests emergency FDA authorization for COVID-19 vaccineA second company is requesting emergency use authorization for a coronavirus vaccine.
Moderna progressing with vaccineModerna filing for emergency use authorization for vaccine.
Moderna seeks U.S., EU vaccine authorization[NFA] Moderna will apply for U.S. and European emergency-use authorization for its COVID-19 vaccine on Monday after full results from a late-stage study showed it was 94.1% effective with no serious..