Emergency use authorizations (EUAs) are one of several tools FDA is using to help make important medical products available quickly during the #COVID19 pandemic. But what exactly is an EUA? | U.S. Food and Drug Administration
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2.8K views · 19 reactions | WebMD Chief Medical Officer Dr. John Whyte speaks with Dr. Peter Marks, Director of the U.S. Food and Drug Administration's Center for Biologics Evaluation and Research, about the FDA's emergency use authorization revisions for convalescent plasma. | WebMD | Facebook
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Today, the FDA launched Elsa, a generative AI tool designed to help employees—from scientific reviewers to investigators—work more efficiently. This innovative tool modernizes agency functions and leverages AI capabilities to better serve the American people. Elsa in Action ➤ Accelerate clinical protocol reviews ➤ Shorten the time needed for scientific evaluations ➤ Identify high-priority inspections targets ➤ Perform faster label comparisons ➤ Summarize adverse events to support safety profile
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5.9K views · 103 reactions | "We're going to continue to gather data, but this clearly meets the criteria that we've established for emergency use authorization, and we're very pleased with these results." -- FDA Commissioner Stephen M. Hahn, M.D., at a White House press conference discussing the convalescent plasma EUA. | U.S. Food and Drug Administration | Facebook
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7.1K views · 53 reactions |  Watch our latest FDA Direct! We discuss: ✅ Major accomplishments including new AI tools for staff ✅ Efforts to modernize drug approval processes ✅ Initiatives to reduce harmful food additives ✅ Plans to combat illegal vaping products ✅ The future of FDA modernization Watch the full conversation: https://www.youtube.com/watch?v=lnx1Ikiawe4&list=PLey4Qe-UxcxbGI04rUjdaGyNhNnuP5cBO | U.S. Food and Drug Administration | Facebook
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7.1K views · 53 reactions |  Watch our latest FDA Direct! We discuss…
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