Didier Caizergues

Head of Regulatory Affairs and Quality Assurance

Généthon

Position in Core Committee - Regulatory Expert

Didier is a pharmacist specialised in Regulatory Affairs and also in pharmaceutical product development.  Since 2001 he has worked for GENETHON where he has successfully obtained Orphan Drugs designations and Clinical Trial Authorisations for gene therapy products in the field of NMD and PID (Pediatric Immunodeficiency) in several European countries. He is responsible for communication with national agencies (Afssaps; MHRA; PEI) the EMEA and the European commission (DG Health and Consumers).

For AFM he has been responsible for successfully preparing and obtaining Clinical Trial Authorisation in France for products which are already on the market in another clinical indication. Previously, he has worked in Regulatory Affairs, in the Pharmaceutical Industry mainly on chemical molecules.