Medical Device Webinars and Stakeholder Calls
The FDA's Center for Devices and Radiological Health (CDRH) hosts webinars and calls to educate stakeholders on guidances and other topics related to the regulation of medical devices and radiation-emitting products. These forums provide the medical device industry and others with the chance to interact with FDA officials and have their questions answered.
This page provides information on upcoming and past webinars and calls held by CDRH. Additional industry education is provided on CDRH Learn.
Webinar - Medical Devices Containing Materials Derived from Animal Sources (Except for In Vitro Diagnostic Devices) Final Guidance - April 23, 2019
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Webinar - Final Guidances on "Deciding When to Submit a 510(k) for a Change to an Existing Device” and “Deciding When to Submit a 510(k) for a Software Change to an Existing Device" - November 16, 2017
Webinar - Final Guidance Documents: “Self-Monitoring Blood Glucose Test Systems for Over-the-Counter Use” and “Blood Glucose Monitoring Test Systems for Prescription Point-of-Care Use” - November 21, 2016