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.
Ask Dr. Nandi: Moderna requests emergency FDA authorization for COVID-19 vaccineA second company is requesting emergency use authorization for a coronavirus 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..
The vaccine created by the companies is known as BNT162b2.
![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)
![Ask Dr. Nandi: Moderna requests emergency FDA authorization for COVID-19 vaccine [Video]](https://video.newsserve.net/300/v/20201130/2011302222-Ask-Dr-Nandi-Moderna-requests-emergency-FDA-authorization.jpg)
![Moderna seeks U.S., EU vaccine authorization [Video]](https://video.newsserve.net/300/v/20201130/2011301838-Moderna-seeks-EU-vaccine-authorization.jpg)
