What Is EUA?
The FDA defines EUA as “an expedited authorization and use of an unapproved product or the off-label use of an already approved product in a declared emergency involving a chemical, biological, radiological, or nuclear (CBRN) agent.
For more info on EUA, see the following thread:
https://hotcopper.com.au/threads/emergency-use-authorization-and-other-approvals.5591703/
MSB to dispute FDA finding in Type A meeting, page-341
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