Agnès Davy

Agnès Davy has extensive experience in regulatory affairs in various medical fields such as hip and knee joint replacement implants, contrast media injection for CT and MRI imaging, population health management, sleep diagnostics, and retinal oximetry. With a background in biomedical engineering, Agnès has managed regulatory activities for product design, development, and market placement, as well as provided regulatory consultancy to medical device manufacturers. Agnès's roles have included managing change control processes, labeling requirements, regulatory pre-market and post-market activities, and quality management systems implementation. Agnès has also gained experience in supporting pre-sales activities, installations, and research projects in the healthcare industry.