Ask Dr. Nandi: Moderna requests emergency FDA authorization for COVID-19 vaccine
A second company is requesting emergency use authorization for a coronavirus vaccine.
Moderna Applies For Emergency FDA Authorization After Successful Vaccine TrialsModerna is the second company in the U.S. to release its full trial results and apply for emergency use authorization.
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..
![Moderna Applies For Emergency FDA Authorization After Successful Vaccine Trials [Video]](https://video.newsserve.net/300/v/20201130/2011302235-Moderna-Applies-For-Emergency-FDA-Authorization-After-Successful.jpg)
![Moderna progressing with vaccine [Video]](https://video.newsserve.net/300/v/20201130/2011302026-Moderna-progressing-with-vaccine.jpg)
![Moderna seeks U.S., EU vaccine authorization [Video]](https://video.newsserve.net/300/v/20201130/2011301838-Moderna-seeks-EU-vaccine-authorization.jpg)
