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Fast Facts

Regulatory I: The IND Phase

Sep 15, 2008 - Sep 17, 2008
Park Hyatt Philadelphia at the Bellevue Philadelphia, Pennsylvania United States
 

Highlights

This course will offer insight into the regulatory background of the IND and outline the content and data requirements for an IND submission to FDA. The course will focus on drug and well-characterized biological products and not the regulatory process for devices, generic products or traditional biologics.

Contact Details

Contact person: Susan Mazak
Email address:
Event website: http://www.diahome.org/DIAHOME/Education/FindEducationalOffering.aspx?productID=16121&eventType=Training%20Course
Phone: +1-215-442-6183

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