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Emergency Use Authorization | FDA The Emergency Use Authorization (EUA) authority allows FDA to help strengthen the nation’s public health protections against chemical, biological, radiological, and nuclear (CBRN) threats
Emergency Use Authorization - Wikipedia On April 16, 2021, the FDA revoked the emergency use authorization (EUA) that allowed for the investigational monoclonal antibody therapy bamlanivimab, when administered alone, to be used for the treatment of mild-to-moderate COVID-19 in adults and certain pediatric patients
What is Emergency Use Authorization (EUA)? ⋆ Brownstone . . . During the Covid pandemic, the U S government spent billions of dollars on nearly 400 products intended to protect, diagnose, and treat hundreds of millions of people – all with the label “EUA” or “Emergency Use Authorization "