[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 to Submit COVID-19 Vaccine for FDA Regulatory Approval.
Moderna will submit its
coronavirus vaccine on Nov. 30.
It is the second drugmaker to ask the FDA
for emergency use..
Credit: Wibbitz Top Stories Duration: 01:03Published
Moderna announced its application to the US Food and Drug Administration for authorization of its COVID-19 vaccine. Veuerβs Maria Mercedes Galuppo has the story.
![Moderna seeks U.S., EU vaccine authorization [Video]](https://video.newsserve.net/300/v/20201130/2011301838-Moderna-seeks-EU-vaccine-authorization.jpg)
![Moderna to Submit COVID-19 Vaccine for FDA Regulatory Approval [Video]](https://video.newsserve.net/300/v/20201130/1313844230-Moderna-to-Submit-COVID-19-Vaccine-for-FDA.jpg)
![Moderna to Ask FDA for Emergency Clearance for Its COVID-19 Vaccine [Video]](https://video.newsserve.net/300/v/20201130/2011301331-Moderna-to-Ask-FDA-for-Emergency-Clearance-for.jpg)
