Principal Regulatory Affairs Specialist
Medtronic, United States
Pamela Campo holds an MS in Regulatory Science and a BA in Sociology, with a decade of experience as a regulatory professional, specializing in medical devices. Currently a Principal Regulatory Affairs Specialist with Medtronic, Pamela applies her critical thinking and technical writing skills to author regulatory submissions and bring diabetes therapy products to the EU market. She also leads the training initiative for EU MDR regulations within the Diabetes operating unit.
Disclosure information not submitted.
Designing Training for an Evolving Regulatory Environment
Thursday, May 11, 2023
13:45 - 14:45 CEST