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Regulatory Affairs Part I: The IND Phase

17 - 19 June 2011, Chicago, United States


Introduction
All You Need to know about IND Submissions in Only 3 Days



Learn how to apply regulatory concepts to ensure compliant IND submissions to FDA. The course focuses on drug and well characterized biological products and not the regulatory process for devices, generic products, or traditional biologics.

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Venue
McCormick Place

McCormick Place, Chicago, United States

Organised by
DIA
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