Sim&Cure
Colette Maurin is a seasoned expert in regulatory affairs and quality assurance, currently serving as Senior Director at SIm&Cure since January 2022, and is a member of the executive committee. With extensive experience in global medical device registration processes, Colette has successfully navigated compliance with international standards such as ISO 13485, 21 CFR, and GDPR across multiple regions including Europe, the USA, Canada, and Asia. Prior roles include Director of Regulatory Affairs and Quality at Intrasense, where Colette also managed human resources, and earlier positions in regulatory and quality management within the medical device sector. Colette's background also includes significant experience in production and quality management in diagnostics, demonstrating a comprehensive understanding of the entire product lifecycle from development to market approval.
This person is not in any teams
Sim&Cure
Sim&Cure is the first company to be cleared to market a patient-based simulation model for aneurysm treatment that allows prediction of the deployment of medical devices (flow diverter, intrasaccular device, laser-cuter stent). Sim&Size® simulates each size and type of device according to the patient’s unique anatomy in order to provideessential information prior to the choice of sizing.