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  1. Workshops & Conferences (Medical Devices)

The CDRH Webinar Program educates stakeholders on guidances, regulations, and various policies for medical devices and radiation-emitting electronic products. The format generally consists of a presentation on a specific topic by an FDA official, followed by an interactive question and answer session with stakeholders. The intended audience for CDRH webinars is regulated industry. 

This page provides information on upcoming and past events. Additional industry education is provided on CDRH Learn and Device Advice.


For a full listing of 2020-2019 webinars visit the FDA.gov Archive


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