The Bench to Bedside Lecture Series by Penn Health-Tech presents Regulatory Basics for Medical Devices. The next session will review regulatory requirements for medical devices, including resources on how to determine your device classification and regulatory pathway and the importance of predicate devices. We will also describe resources available within Penn’s Office of Clinical Research for early clinical evaluation of new technologies.

Featured Guest

Monica Ferrante, DPA
VP of Regulatory, Quality, and Clinical,
Vitara