Director
Philips Healthcare
Meg Mucha has over 30 years of quality and regulatory experience for pharmaceuticals and medical devices. Meg's roles have included direction for the quality control/assurance and regulatory affairs for active pharmaceutical ingredients and medical devices. Meg has held roles as Director of Regulatory Affairs for GE Healthcare and Mortara Instruments (aka Baxter) where she was responsible for the global market authorization of medical devices. Meg was the COO for RAQA and BISO at IBM Watson Health. She is currently the Director of Q&R Audit and Compliance leading the internal audit activities at Philips Healthcare.
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Tuesday, September 13, 2022
3:30 PM – 4:30 PM MST