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Kendle Appoints Former MHRA Head of Biologics as Principal Regulatory Affairs Consultant
Date:12/20/2007

ues, and represented the United Kingdom on the Biologics Working Party of the Committee for Medicinal Products for Human Use (CHMP) at the European Medicines Agency (EMEA). He also worked as Senior Director, Head of European Regulatory Affairs for Shire Human Genetic Therapies, Ltd. Prior to that, Dr. Forsey worked for Pharmacia, Amgen, the National Institute for Biological Standards and Control and the University of London. In all, he brings more than 30 years of pharmaceutical, governmental and research experience to his role with Kendle.

Dr. Forsey earned a doctorate in microbiology from the University of London and a Bachelor of Science in microbiology from the University of Surrey, England. A widely-published author, he is a registered member of The Organisation for Professionals in Regulatory Affairs (TOPRA) and the Drug Information Association (DIA).

Dr. Forsey is the latest member of an international team of pharmaceutical, clinical and non-clinical biotechnology experts Kendle has assembled with backgrounds encompassing regulatory agencies on three continents, as well as experience working for a variety of pharmaceutical companies and academic and research institutions.

About Kendle

Kendle International Inc. (Nasdaq: KNDL) is among the world's leading global clinical research organizations and is the fourth-largest provider of Phase II-IV clinical development services worldwide. We deliver innovative and robust clinical development solutions - from first-in-human studies through market launch and surveillance - to help the world's biopharmaceutical companies maximize product life cycles and grow market share.

Our global clinical development business is focused on five regions - North America, Europe, Asia/P
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