On September 20, 2023, Rebecca McKnight serves as an instructor for the Food & Drug law Institute’s Training Program for FDA’s Center for Devices and Radiological health (CDRH). The goal of this program is to increase the knowledge and understanding of CDRH staff on the legal and regulatory issues related to medical device law and how FDA regulates the medical device industry. Rebecca provided and interactive presentation and training session on Informed Consent, Institutional Review Boards (IRBs), and Protection of Human Subjects in Medical Device Research.

Speakers: Rebecca Jones McKnight

Event Type: Webinar

Start Date/Time:
20 September 2023