Camille Piriou

Camille Piriou

Senior Consultant, Regulatory Affairs

Key Knowledge Areas:

-European procedures,
- 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.

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