With over 20 years of experience in the medical device field, in various roles (R&D, Regulatory Affairs, Project Manager, Technical file reviewer - as a consultant or in a permanent position), working with different types of medical devices (silicone implants, electromedical imaging devices, dental products), and within various types of organizations (small, medium, or large companies - manufacturers, Notified Bodies - Paris area, South of France), I have developed solid expertise that enables me to support medical device manufacturers with their regulatory projects, whether occasional or recurring.