Regulatory Education for Industry (REdI) Annual Conference
June 6-10 – Register for this conference on topics including 510(k)s, inspections, and regulatory responsibilities.
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Webinar on Proposed Rule for Establishing Over-the-Counter Hearing Aids and Draft Guidance for Regulatory Requirements for Hearing Aid Devices and Personal Sound Amplification Products - December 7, 2021
Webinar - Consideration of Uncertainty in Making Benefit-Risk Determinations in Medical Device Premarket Approvals, De Novo Classifications, and Humanitarian Device Exemptions: Final Guidance - October 16, 2019