Florianne Torset-BonfillouDirector, Compliance Department at GMED North America
Florianne is the Director of the Compliance Department at GMED North America. She has a background in Biology, Chemistry and Quality Management. After working in the Pharma/Device industry, Florianne first joint GMED as an Assessor. She is a Lead Auditor and Senior Product Reviewer with focus on high risk devices, mainly in the cardio and neurovascular field.
Florianne provides Regulatory support to the local team and is currently focusing on the transition to the European Regulation EU 2017/745 and EU 2017/746.
She is also a trainer on the European Regulation, Quality Management, Risk Management, and other regulatory and quality topics.