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Webinar - Remanufacturing of Medical Devices Draft Guidance and Strengthening Cybersecurity Practices Associated with Servicing of Medical Devices Discussion Paper - July 27, 2021
TAKE OUR SURVEY - Tell us what you think about the webinar
Webinar Series - Respirators and Other Personal Protective Equipment (PPE) for Health Care Personnel Use During the COVID-19 Pandemic - July 13, 2021
TAKE OUR SURVEY - Tell us what you think about the webinar
Webinar - Testing and Labeling Medical Devices for Safety in the Magnetic Resonance (MR) Environment - June 24, 2021
TAKE OUR SURVEY - Tell us what you think about the webinar
Webinar - ASCA Pilot: Streamlining Conformity Assessment in Device Submissions - May 20, 2021
TAKE OUR SURVEY - Tell us what you think about the webinar
Webinar Series - Respirators and Other Personal Protective Equipment (PPE) for Health Care Personnel Use During the COVID-19 Pandemic - April 27, 2021
TAKE OUR SURVEY - Tell us what you think about the webinar
Webinar Series - Respirators and Other Personal Protective Equipment (PPE) for Health Care Personnel Use During the COVID-19 Pandemic - February 23, 2021
TAKE OUR SURVEY - Tell us what you think about the webinar
Webinar - Safer Technologies Program: Final Guidance - February 1, 2021
TAKE OUR SURVEY - Tell us what you think about the webinar
Webinar Series - Respirators and Other Personal Protective Equipment (PPE) for Health Care Personnel Use During the COVID-19 Pandemic - January 26, 2021
TAKE OUR SURVEY - Tell us what you think about the webinar
Virtual Town Hall Series - Coronavirus (COVID-19) Test Development and Validation - December 16, 2020
TAKE OUR SURVEY - Tell us what you think about the webinar
Webinar Series - Respirators and Other Personal Protective Equipment (PPE) for Health Care Personnel Use During the COVID-19 Pandemic - December 8, 2020
TAKE OUR SURVEY - Tell us what you think about the webinar
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
Webinar - Special 510(k) Program Pilot - November 8, 2018
Webinar - Appropriate Use of Voluntary Consensus Standards; Final Guidance - October 25, 2018
Webinar - Quality in 510(k) Review Program Pilot - October 10, 2018
Webinar - FDA Innovation Challenge: Devices to Prevent and Treat Opioid Use Disorder - July 25, 2018
Webinar - Final Guidances on Next Generation Sequencing-based Tests - May 24, 2018
User Session - Digital Health Software Precertification (Pre-Cert) Pilot Program - May 10, 2018
Webinar - Duodenoscope Sampling and Culturing - March 22, 2018
Webinar - Custom Device Annual Reporting - February 27, 2018
Webinar - Technical Considerations for Additive Manufactured Medical Devices - January 10, 2018
Webinar - PreCertification (Pre-Cert) Pilot Update - November 17, 2017
Webinar - CDRH Final Guidance: Qualification of Medical Device Development Tools - August 24, 2017
Optimizing GUDID Data Quality- August 3, 2017
Webinar - Digital Health Software Precertification (PreCert) Pilot Program - August 1, 2017
Webinar - Final Guidance on Medical Device Reporting for Manufacturers - November 30, 2016
Webinar - CDRH Industry Basics Workshop: The Quality System - November 3, 2016
Webinar - Final Guidance on Patient Preference Information - September 27, 2016
Webinar - Final Guidance on "General Wellness: Policy for Low-Risk Devices" - September 1, 2016
Webinar - An Update on the FDA's Medical Device Clinical Trials Program - July 14, 2016
Artificial Pancreas: A Dialogue between the FDA and the Diabetes Community - June 2, 2016
Applying Human Factors and Usability Engineering to Medical Devices - February 19, 2016
Color Additives for Medical Devices - February 12, 2016
CDRH Industry Basics Workshop - Unique Device Identification (UDI) - January 27, 2016