Mes compétences :
Affaires réglementaires
Conseil
EMEA
Europe
Institutions européennes
OMS
Principes actifs
Qualité
Quality
Entreprises
EGA
- Director, Quality & Regulatory Affairs
2015 - maintenant
European Generic medicines Association
- Sr Manager Regulatory Affairs
2007 - 2014In my current position, interactions with EU institutions on the development or update of legislative texts (dealing with scientific & technical aspects of the pharmaceutical legislation) have considerably broadened my understanding of the various EU legislative processes, and the impact laws, rules and guidelines can have on day-to-day business and the way these are or should be implemented by the industry.
In the future, I am looking at actively contributing to EU legislative consultation processes in view of changes in order to help law come closer to industry day-to-day but also to ensure the proper safeguards are there to ensure safe and accessible medicines and technology.
Baxter World Trade
- Sr RA Associate European IV Therapy
2005 - 2007
Consultant Industrie Pharmaceutique
- Head of Pharmaceutical Development
