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What is an emergency use authorization and how is it being used to respond to COVID-19?  


Developing and Manufacturing Drugs, Including Biologics, for Treating or Preventing COVID-19
(@mayabailey)
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For certain types of emergencies, the FDA may issue emergency use authorization, or EUA, to provide more timely access to critical medical products (including medication and testing) that may assist during an emergency when there are no available, approved, and available options.

The EUA process is different from FDA approval, approval, or licensing because EUA standards may allow for data-based approvals that are much lower than those required by FDA approval, approval, or licensing. This allows the FDA to authorize the urgent use of medical products that meet the procedure within weeks rather than months to years.

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