Senior Consultant, Regulatory Affairs and Intelligence
Florence has a broad experience in regulatory affairs including development and life cycle management activities for medicines gained through a number of positions in the pharmaceutical industry over the past 12 years.
Florence has been involved in various regulatory projects assisting start-up to international companies. Her recent client work includes:
Florence has recently enlarged her responsibilities by overseeing Regulatory intelligence at Bluereg. She is actively ensuring the up-to-date internal knowledge of Bluereg consultants by providing routinely latest regulatory news and providing highlights or training on specific regulatory topics or novel legislation. She is also supporting consultants by providing regulatory analysis on client’s specific request.
Background / Past experience
Florence earned her Pharm.D. degree from the University of Pharmacy in Clermont-Ferrand, France.
Prior to joining Bluereg, Florence worked for several companies in Paris, in the UK and in the South of France. During her past positions, Florence has been covering a wide range of regulatory activities for registration of medicines in France and EU. She has also covered other activities including registration of medicines and devices in Asian and Maghreb countries, control of promotional materials for FR and UK market, due diligences. She has also been involved in pharmacovigilance activities.