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PAREXEL Consulting Enhances European Regulatory Affairs Capabilities With Appointment of Medical Products Agency Expert Dr. Anders Neil
Date:2/17/2009

L's consulting experts are recognized for managing successful interactions with regulatory agencies, delivering world-class submissions, and helping biopharmaceutical companies define and execute the most efficient paths to approval," said Dr. Neil. "I am proud to join such a high caliber team of experts to help clients with scientific decisions, especially early in development planning, and with regulatory approaches to achieve first-cycle approval."

Dr. Neil was appointed as Senior Expert by MPA in 2005, following his long-term role as MPA Team Leader. During his tenure at MPA Dr. Neil assessed marketing authorizations and clinical trial applications, including nonclinical and pharmacology aspects of more than 1,000 applications spanning all stages of development and therapeutic areas. He has served as an expert to the European Committee for Proprietary Medicinal Products (CPMP), now the Committee for Medicinal Products for Human Use (CHMP), and to its Safety Working Party as a rapporteur on European Union (EU) regulatory documents. Dr. Neil was also appointed to the EU Commission's list of scientific experts on emerging and newly identified health risks. Dr. Neil is currently an Associate Professor of Pharmacology at Uppsala University in Sweden.

For more information about PAREXEL Consulting's full capabilities and areas of expertise, visit: http://www.parexelconsulting.com.

About PAREXEL Consulting

PAREXEL Consulting, a division of PAREXEL International, provides integrated product development services with the goal of helping biopharmaceutical and medical device companies get their products to the market, and keep them on the market. Through a unique fusion of scientific, regulatory, and business expertise PAREXEL Consulting helps clients worldwide manage risk and maximize product and portfolio value at every milestone and
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