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. The intended audience for CDRH webinars is regulated industry.
Webinar on Proposed Rule for Establishing Over-the-Counter Hearing Aids and Draft Guidance for Regulatory Requirements for Hearing Aid Devices and Personal Sound Amplification Products - December 7, 2021
For a full listing of 2020-2019 webinars visit the FDA.gov Archive