Pierre Poitou has worked for more than 30 years in various pharmaceutical companies, including Pierre Fabre, Lederle (before the merger with Wyeth, now part of Pfizer), Servier and Takeda (until June 2010). From 2000 to 2003, he has been VP Worldwide Regulatory Affairs (South Europe) of the CRO Parexel. His experience covers scientific, technical and regulatory aspects of healthcare products, in France and Europe, including market access and compliance issues.
Pierre is now a Freelance Consultant, and a member of the French National Academy of Pharmacy.
Key words: Regulatory compliance, Product development and strategy, Licensing, Market access, Quality issues.
Medicines and other health...
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