FDA revamps adverse event reporting guidance for Covid-19 – Endpoints News

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The FDA on Thursday revised its guidance on postmarket adverse event reporting for medical products and dietary supplements during a pandemic to apply the guidance to the ongoing coronavirus disease (Covid-19) pandemic.

The guidance, which applies to drugs, biologics, medical devices, combination products and supplements, details how FDA intends to prioritize adverse event reporting requirements during a pandemic.

Click here to read full article https://endpts.com/fda-revamps-adverse-event-reporting-guidance-for-covid-19/

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