Regulatory Science, Drugs and Biologics
Julie Taccoen joined Voisin Consulting Life Sciences (VCLS) in 2007 and participates in the design and implementation of Regulatory Strategies for the Development of Drugs and Innovative Medicinal Products. She has extensive experience in the preparation of scientific advice and drug regulatory applications at national and European level (Centralized, Mutual Recognition and decentralized procedures) as well as in the life cycle management of approved medicinal products.
Julie manages the post-marketing pharmacovigilance activities linked to the life cycle management of medicinal products in Europe, including the preparation of Risk Management Plans and Periodic Safety Update Reports. She also has experience in the management of compassionate use programmes in Europe.
Julie gained previous international experience as Assistant to the Scientific Attaché of the French Consulate in Shanghai, China, in charge of the Life Sciences Sector. For a two year period, Julie was in charge of advising Scientific Researchers and following the Scientific and Regulatory development in China. She also gained experience in the field of Molecular Biology during a six-month internship at Zensun, an R&D Biopharmaceutical Company based in Shanghai, China, and in the field of cell biology working on the effects of estrogens on male fertility at INSERM (French National Institute for Health and Medical research).
Julie obtained her Masters Degree (Engineering) in Biotechnology and Biochemistry from INSA (Institut National des Sciences Appliquées) in Lyon, France. INSA provides a comprehensive program in mathematics, physics, mechanics, chemistry, and a three-year intensive major in biotechnology-biochemistry.