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Florianne Torset-Bonfillou, MS, RAC

Senior International Regulatory Project Manager
GMED North America

Florianne is a Senior International Regulatory Project Manager at GMED North America. She is also a Lead Auditor and a Product Reviewer with focus on high-risk devices, mainly in the cardio and neurovascular fields.
With over 15 years of experience in the Medical Devices Regulatory Affairs, Florianne brings an extensive experience as assessor, trainer and support team for the implementation of the European Medical Device Regulations. For the past 5 years, Florianne provided Regulatory support to the GMED teams for the transition to the European Regulation EU 2017/745 and EU 2017/746. Since 2023, she supports the UK subsidiary towards its UKCA designation.
She is also a trainer on the European Regulation, Quality Management, Risk Management, and other regulatory and quality topics.

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