Key Knowledge Areas:
Pharmacist Doctorate from Rennes University – 2011
Master’s Degree in Regulatory Affairs from Chatenay Malabry University – 2010
Camille has a broad experience in regulatory affairs gained through a number of positions in the pharmaceutical industry over the past 10 years.
Camille has been involved in various regulatory projects assisting SME to international companies as regulatory affairs project manager.
During 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.
In 2018, 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 BlueReg.