
Moderna Filles for Emergency Use Authorization From the FDA for Its Vaccine Candidate
Ndey Manneh
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<p>Moderna has now become the second company to request emergency use authorization from the FDA for their vaccine candidate. In their latest findings, the vaccine is over 94% effective against coronavirus and very effective at preventing serious cases of the virus. The next step will be on Dec. 10 when the FDA will discuss approval for Pfizer and then Dec. 17 for Moderna. Karen Weintraub, health reporter at USA Today, joins us for more as we get closer to vaccine approvals.</p><p> </p> Learn more about your ad-choices at <a href="https://www.iheartpodcastnetwork.com">https://www.iheartpodcastnetwork.com</a><p>See <a href="https://omnystudio.com/listener">omnystudio.com/listener</a> for privacy information.</p>
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Moderna Filles for Emergency Use Authorization From the FDA for Its Vaccine Candidate
Ndey Manneh