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- ICYMI - Updates from the FDA on the EUA Process
The CAP hosted a webinar to discuss updates to the Food and Drug Administration (FDA) Emergency Use Authorization (EUA) process on October 25. The FDA’s Timothy Stenzel, MD, PhD, who is the Director of the FDA Office of In Vitro Diagnostics and Radiological Health, and Toby Lowe who is the Associate Director for Regulatory Programs in Office of In Vitro Diagnostics and Radiological Health, provided pathologists with an overview of current EUA processes and answered questions.
Check out the recording and download the slides.