CDRH Events

This page provides information on medical device webinars, town halls, meetings (FDA sponsored and FDA Co-Sponsored), and workshops. 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.

For a full list of all FDA meetings visit FDA Meetings, Conferences and Workshops. For information about Advisory Committee meetings visit Advisory Committees or the Advisory Committee Calendar.

Date	Event Type	Event
02/07/2024	Town Hall	Medical Device Sterilization Town Hall: Discussion of Premarket Submission Expectations and Additional Considerations for Sterility Review
01/26/2024	Town Hall	Medical Device Sterilization Town Hall: FDA Activities and Challenges in Reducing Reliance on Ethylene Oxide (EtO)
01/11/2024	Webinar	Assessing the Credibility of Computational Modeling and Simulation in Medical Device Submissions Final Guidance
01/10/2024	Town Hall	Medical Device Sterilization Town Hall: Overview of Sterilization Landscape and Role of Ethylene Oxide

Events Held in Prior Years

Date	Event Type	Event
12/12/2023	Webinar	Oncology Drug Products Used with Certain In Vitro Diagnostic Tests: Pilot Program
12/05/2023	Webinar	Immediately-in-effect guidance: Antimicrobial Susceptibility Test System Devices - Updating Breakpoints in Device Labeling
11/28/2023	Conference	UGA/FDA 10th Annual Medical Device Regulations Conference
11/14/2023	Webinar	Breakthrough Devices Program Updated Final Guidance
11/02/2023	Webinar	Final Guidance: Cybersecurity in Medical Devices: Quality System Considerations and Content of Premarket Submissions
11/02/2023	Virtual Public Workshop	Extended Reality in Orthopedic Surgical Devices: Insights into User Experience and Adverse Event Reporting for Patient Safety
10/31/2023	Webinar	Proposed Rule: Medical Devices; Laboratory Developed Tests
10/26/2023	Webinar	CDRH's New Draft Guidances to Continue to Modernize the 510(k) Program
10/12/2023	Webinar	Use of International Standard ISO 10993-1, "Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process" - Final Guidance
09/29/2023	Virtual Public Workshop	Patient-Reported Outcomes and Vision Related Quality of Life Questionnaires
09/14/2023	Webinar	Clinical Considerations for Studies of Devices Intended to Treat Opioid Use Disorder - Draft Guidance
09/12/2023	Webinar	Qualification of Medical Device Development Tools
07/20/2023	Webinar	Final Guidance: Content of Premarket Submissions for Device Software Functions
04/26/2023	Virtual Town Hall	Test Development and Validation During the COVID-19 Public Health Emergency
04/18/2023	Webinar	Webinar on Guidances on COVID-19 Transition Plans for Medical Devices
04/13/2023	Webinar	Marketing Submission Recommendations for a Predetermined Change Control Plan for Artificial Intelligence/Machine Learning-Enabled Device Software Functions Draft Guidance
03/22/2023	Virtual Town Hall	Test Development and Validation During Public Health Emergencies Monkey pox (mpox) and COVID-19
02/15/2023	Virtual Town Hall	Test Development and Validation During Public Health Emergencies Monkey pox (mpox) and COVID-19
02/02/2023	Webinar	Electromagnetic Compatibility (EMC) of In Vitro Diagnostic Devices
01/11/2023	Virtual Town Hall	Test Development and Validation During Public Health Emergencies Monkey pox (mpox) and COVID-19

U.S. Food and Drug Administration

CDRH Events

Events Held in Prior Years

Other Meeting Resources