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Date: 9th July, 2009

Location: On-Line, Canada

Summary:
Clinical, Pharmaceutical - Web Seminar

Instructor: Frank S. Kohn, PhD

Discussion Points will include:

-Learn about global regulation requirements for EM
-Review the various guidelines on EM
-Understand how to track and trend data
-Learn what are the key validation issues with EM programs
-Provide information on quality systems and risk analysis