Bench2Market Talk: Medical Device and IVD Regulatory Overview
Have you ever wondered what it takes to take a medical technology through the FDA? Regulatory strategy can be complicated, but there are resources to help. Join us on February 15 for a discussion on FDA regulatory strategy featuring Sandra Maher, MS, a regulatory affairs professional specializing in medical devices and diagnostics. She worked on the NIH Rapid Acceleration of Diagnostics (RADx) Initiative for COVID-19. Come ready with questions!