Senior Consultant, Regulatory Affairs
- OTC switches procedures,
- Life Cycle Management,
- Promotional material validation
Pharmacist Doctorate held in Rennes University – 2011
Master Degree in Regulatory Affairs held in Chatenay Malabry University – 2010
In the last 9 years, Camille held several positions at Galderma R&D in the regulatory affairs team. Her last role was Self-Medication Regulatory Affairs Officer, with a worldwide responsibility on a complete range of OTC and prescription, cosmetics & medical devices. She has expertise in a wide range of regulatory activities including registrations, lifecycle management, OTC switches, validation of promotional material.
More recently, she was Regulatory Affairs Manager at the UK trade association of OTC/food supplements & medical devices manufacturers, PAGB, based in London.
In September 2018, Camille moved to consultancy and joined Blue Reg Europe.