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Regulation, Clinical and Software for Medical Devices
November 5 - 7, 2024
The Royal Sonesta Minneapolis DowntownMinneapolis, Minnesota

Florianne Torset-Bonfillou
Sr International Regulatory Project Manager at GMED North America


Florianne is a Senior International Regulatory Project Manager at GMED North America. For the past 5 years, Florianne provided Regulatory support to the local teams for the transition to the European Regulation EU 2017/745 and EU 2017/746 and UKCA designation.

She is also a Lead Auditor and a Product Reviewer with focus on high-risk devices, mainly in the cardio and neurovascular field.

She has a background in Biology, Chemistry and Quality Management. After working in the Pharma/Device industry, Florianne first joint GMED as an Assessor, then became part of the Quality & Regulatory support team.

She is also a trainer on the European Regulation, Quality Management, Risk Management, and other regulatory and quality topics.

Agenda Sessions

  • Accessing UK Market – Current and Upcoming State of the UK Medical Device Regulation