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Webcast

March 9, 2010

Hurdles and Pitfalls in Generic Drug Development

You will learn how to plan and conduct a bioequivalence study and how to report PK data for the approval of generic drugs.

Webcast length: 1 hour 14 minutes

To view the webcast Click here

 

About PAREXEL

PAREXEL is a leading global bio/pharmaceutical services organization that helps clients expedite time-to-market through our development and launch services. These include a broad range of clinical development capabilities, integrated advanced technologies, regulatory affairs consulting, and commercialization services.