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 - Digital Health Center of Excellence Listening Session #2 - November 12, 2020
Webinar - Digital Health Center of Excellence Listening Session #1 - October 19, 2020
Webinar - Multiple Function Device Products: Policy and Considerations - September 10, 2020
Webinar Series - CDC/NIOSH's Surgical N95 Respirator Guidance - September 1, 2020
Webinar Series - FDA’s Surgical Masks Umbrella EUA - August 26, 2020
Webinar Series - Respirators for Health Care Personnel Use during COVID-19 Pandemic - July 21, 2020
Webinar Series - Respirators for Health Care Personnel Use during COVID-19 Pandemic - July 7, 2020
Webinar Series - Respirators for Health Care Personnel Use during COVID-19 Pandemic - June 23, 2020
Webinar Series - Respirators for Health Care Personnel Use during COVID-19 Pandemic - June 9, 2020
Virtual Town Hall - 3D Printed Swabs - May 15, 2020
Webinar - 510(k) Third Party Review Program: Final Guidance - April 16, 2020
Webinar - Safety and Performance Based Pathway Performance Criteria - November 7, 2019
Webinar - Safer Technologies Program: Draft Guidance - November 6, 2019
Webinar - Clinical Decision Support Software: Draft Guidance - November 4, 2019
Webinar - The Special 510(k) Program: Final Guidance - October 31, 2019
Webinar - Collaborative Communities - October 29, 2019
Webinar - Humanitarian Device Exemption Program - October 21, 2019
Webinar - Dental Devices Premarket Submissions - October 2, 2019
Webinar - Acceptance Review for De Novo Classification Requests: Final Guidance - September 18, 2019
Webinar - Q-Submission Program for Medical Device Submissions - June 11, 2019
Webinar - Unique Device Identification: Convenience Kits Final Guidance - May 21, 2019
Webinar - The Least Burdensome Provisions: Concept and Principles Final Guidance - March 14, 2019
User Session - Digital Health Software Precertification (Pre-Cert) Pilot Program - February 7, 2019
Webinar - Breakthrough Devices Program Final Guidance - January 17, 2019
Webinar - CLIA Waiver Applications Draft Guidances - January 9, 2019