[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
AstraZeneca and the University of Oxford are facing criticism over their COVID-19 vaccine trial results.
According to Business Insider the criticism comes after AstraZeneca admitted to a mistake in..
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