RAQA Executive, Quality Management System Medical Devices
Margaret (Meg) Mucha has over 20 years of quality and regulatory experience for pharmaceuticals and medical devices. Meg’s roles have included direction for the quality control/quality assurance and regulatory affairs for active pharmaceutical ingredient manufacturers and RA Director for GE Healthcare and Mortara Instrument where she was responsible for global market authorization of medical devices for cardiology and radiology products both 510(k) and PMA. In her current role, Meg manages a global team of 40 who are responsible for the quality assurance, premarket, and post market regulatory affairs activities for Watson Health Imaging products.
Tuesday, September 15, 2020
11:00 AM – 12:30 PM EDT
Wednesday, September 16, 2020
10:35 AM – 11:30 AM EDT