DIRECTOR REGULATORY AFFAIRS & QUALITY
Luc Morisset has more than 20 years of experience in EU regulatory affairs. He is a graduate from UTC University in Compiegne, France and holds a degree in biomedical engineering.
Luc started his career as a hospital biomedical engineer and then moved to the French Ministry of Health, where he was in charge of pre-market approval for specific devices in France. Before joining STENTYS in 2007, Luc was Director of Regulatory Affairs for 11 years at MedPass International, a CRO specialized in medical devices, where he helped numerous companies by developing regulatory strategies to expedite CE marking and clinical trial approvals in the European Union.