Director Business Development
- Regulatory Affairs
- Management of post MA activities
(promotional review, Charte Visite Médicale)
Carole is a pharmacist and completed her Pharmaceutical education at the University of Marseille, France (2001). She also obtained a Master Degree in Regulatory Affairs Health Industry at the University of Sceaux (2001).
Carole has more than 15 years of experience in Regulatory Affairs, especially in the field of registration (France, Europe) and management of post-MA activities.
During her first experiences within Janssen-Cilag France and Boehringer-Ingelheim France, Carole has developed her regulatory expertise and it has much contributed to developing her skills in terms of sharing information, working in project team organization.
Then she moved to Laboratoires Genévrier helding the position of Regulatory Affairs Manager for medicinal products. She managed registration procedures (MRP, DCP and national procedures) and was participating to development program for new drugs, including participation in scientific advice meeting with European Agencies. Carole also performed other activities related to Regulatory Department such as annual site report, and advertising control.
After 13 years of experience in the Pharmaceutical industry, Carole moved to consultancy and joined BlueReg in September 2013.