Dr. Fatima Sanfourche serves as the Global Sr. Director of QA & RA Compliance for Medical Devices, Combination Products, and eHealth at Bayer since January 2017, with a focus on ensuring regulatory compliance for Bayer Pharmaceuticals’ quality management system. In addition to leading the implementation of EU MDR across the organization, Dr. Sanfourche has held various roles in quality and regulatory affairs, including the President of Feminin Pluriel Berlin and previous positions at Penumbra Europe GmbH, Thermo Fisher Scientific, and GenPat77 Pharmacogenetics AG. Dr. Sanfourche's educational background includes a Ph.D. in Pharmacology and Pharmacochemistry from the University of Strasbourg, complemented by a Master’s degree from the same institution and additional coursework at Lund University.
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