Emergency Use Authorization by U.S. FDA

E1977494 UNEXPLORED

Emergency Use Authorization by the U.S. FDA is a regulatory mechanism that allows the agency to permit the use of unapproved medical products or unapproved uses of approved products during public health emergencies when certain criteria are met.

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Label Occurrences
Emergency Use Authorization by U.S. FDA canonical 1

Referenced by (1)

Full triples — surface form annotated when it differs from this entity's canonical label.

BNT162b2 hasRegulatoryApproval Emergency Use Authorization by U.S. FDA