Skip to main content
RAPS Euro Convergence 2024 Main banner
Icon Legend
This session is not in your schedule.
This session is in your schedule. Click again to remove it.
Presentation Icons
Ticketed Event
Ticketed Event
Sponsored Presentation
Sponsored Presentation
Learning Level: Foundational
Learning Level: Foundational
New Exhibitor
New Exhibitor
Networking Event
Networking Event
Enterprise Network Member
Enterprise Network Member
Learning Level: Expert
Learning Level: Expert
Learning Level: Advanced
Learning Level: Advanced
Learning Level: Intermediate
Learning Level: Intermediate
Back

Christelle Bouygues, PharmD

Senior Regulatory Affairs Specialist
EMA

Senior Regulatory Affairs Specialist at the European Medicines Agency. The EMA Regulatory Affairs Office is responsible for providing regulatory intelligence and advice in relation to the development, evaluation and surveillance of medicinal products for human use submitted through the Centralised Procedure (including scientific advice, orphan, paediatric, SME) and to its Committees.
Christelle was involved in particular with the implementation of the paediatric and pharmacovigilance legislation. Currently, amongst other projects, Christelle is closely involved in the implementation of the MDR/IVDR within EMA as regard to the aspects on medical devices used in combination with medicinal products. Before joining the Agency, I gained a 4-year experience at the French Competent Authority, in the Mutual Recognition Procedures and the Oncology Evaluation services, and had a 2-year experience in the pharmaceutical industry.

Disclosure information not submitted.

Presentation(s):