Bio :

Cécile Vaugelade, a chemical engineer by training, began her career at the french sanitay agency in the field of medical device reimbursement and then in medical device market surveillance (market control, vigilance, regulatory affairs, clinical trial authorization, etc.). She then worked at LNE/G-MED, a French notified body, as head of the G-MED certification center for over three years before joining SNITEM as Director of Regulatory Affairs in 2018.
At SNITEM, she is responsible for managing regulatory activities covering a wide range of topics (CE marking, advertising, clinical investigations and evaluations, health vigilance, environmental regulations, end of life of medical devices, standardization, etc.).