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Afficher les exemplaires de cette édition ISBNon international cooperation, convergence, and harmonization of regulations for pharmaceutical
and biotechnology products. He has worked in different cultural environments and lived in
both Europe and the United States.
Dr. Lezotre studied biology (University of Sciences, Saint-Etienne, France)
and drug development (University of Pharmacy, Montpellier, France) from
1992 to 1998. He then received his Master in Regulatory Sciences in 1999 (University
of Pharmacy, Lille, France). He also recently completed his PhD in Law with honors (Doctoral
School of “Law, Politics and Management, University of Law, Lille, France).
Since 1998, Dr. Lezotre has worked for several international pharmaceutical and biotechnology
companies, with increasing levels of responsibility. He has served as a regional and
then global regulatory leader for small molecule and biologic/biotech programs in various
stages of research and development (from early discovery to life cycle management). He
successfully led many global regulatory teams in supporting global registrations of major
products and numerous development projects in several therapeutic areas, including
dermatology, urology, neurology, and pain. He has been responsible for communications
with worldwide Drug Regulatory Authorities and has also worked with external partners/
companies through co-development agreements and business development programs.
Dr. Lezotre has recently been invited to teach courses on international regulation in the
Regulatory Sciences programs of the University of Southern California (USC).
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