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Regulatory I: The IND Phase

15 - 17 September 2008, Philadelphia, PA, United States


Introduction
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.

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Venue
Park Hyatt Philadelphia at the Bellevue

Park Hyatt Philadelphia at the Bellevue, Broad and Walnut Streets, Philadelphia, PA, 19102, United States

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Organised by
Drug Information Association
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