Samuel Buet

Samuel Buet is a seasoned consultant manager specializing in medical devices with extensive experience in regulatory affairs and product management within the MedTech sector. Currently at STRATEGIQUAL SAS and ProductLife Group, Samuel Buet conducts regulatory projects, focusing on MDR/IVDR certifications and compliance for medical device manufacturers. Previously, as Regulatory Affairs Manager for Mayoly Spindler, Samuel developed global regulatory strategies and managed international registrations. Earlier roles include Product Manager at Takara Bio Europe, leading the launch of in vitro diagnostic solutions, and Regulatory and Quality consultant at STRATEGIQUAL SAS, where Samuel developed market access strategies. Samuel holds a Doctor of Pharmacy from Université Paris-Saclay and a Master's in Quality Management from Université de Bordeaux.