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, to answer technical questions on the development and validation of certain tests, 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 - Proposed Rule: Medical Devices; Laboratory Developed Tests - October 31, 2023
Webinar - CDRH's New Draft Guidances to Continue to Modernize the 510(k) Program - October 26, 2023
Webinar - Qualification of Medical Device Development Tools - September 12, 2023
Webinar on Guidances on COVID-19 Transition Plans for Medical Devices - April 18, 2023
Webinar – Electromagnetic Compatibility (EMC) of In Vitro Diagnostic Devices - February 2, 2023
For a full listing of 2020-2019 webinars visit the FDA.gov Archive