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PAREXEL Experts to Present Leading Insights at Drug Information Association 21st Annual Euromeeting
Date:3/5/2009

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Monday, March 23

  • The PSUR: A Pharmacovigilance and Medical Writing View with Emphasis on Practical Solutions to The Pitfalls and Grey Areas (tutorial) - Alison Rapley, B.Sc., Director, Clinical Research Services (9:00)

Tuesday, March 24

  • Integration of Technology: Today's Fad or Tomorrow's Standard? - Bill Byrom, Ph.D., Vice President, Product Strategy, Perceptive Informatics (9:00)
  • ePRO Soup to Nuts: The Application of ePRO in Clinical Trials - Keith Wenzel, Senior Director, Product Management, ePRO, Perceptive Informatics (11:00)
  • Process Validation During Clinical Development of Biological Medicinal Products - Cecil Nick, B.Sc. (Hons), Vice President, Biotechnology, PAREXEL Consulting (14:00)
  • Doing the Project Planning for Large Multinational Clinical Trials - Diego Martin Glancszpigel, Vice President, Latin America Operations (14:00)
  • A Risk-Based Approach to Supplier Selection - Siegfried Schmitt, Ph.D., Principal Consultant, PAREXEL Consulting (16:00)
  • A Global Programme for the Next Generation in Biosimilars - Session Chair: Cecil Nick, B.Sc. (Hons), Vice President, Biotechnology, PAREXEL Consulting (16:00)

Wednesday, March 25

  • Borderlines: Don't Fence Me In - Peter Lassoff, Pharm D, Vice President, Europe, PAREXEL Consulting (9:00)
  • Selecting Promising New Compounds Earlier by Tapping into Modern Safety and Pharmacological Mechanism in Early Exploratory Clinical Research - Matthias Grossman, M.D., Ph.D., Vice President and Principal Consultant, Early Development (9:00)
  • The Next Generation of EDC Integration - David Stein, Vice President, Product Management, Perceptive Informatics (9:00)
  • Medical Devices and Drug Device Combinations - Esth
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