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Navigating 91AV, Manufacturing and Controls through the Drug Development Process

10 - 11 September 2012, Horsham, United States


Introduction
Participants in this course will learn how to write and assemble the 91AV, Manufacturing and Control (CMC) sections of regulatory submissions. Learners will also be prepared for CMC meetings with the US Food and Drug Administration (FDA) and be taught how to avoid noncompliance.
EVENT CODE:12436

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Venue
DIA

DIA, Enterprise Drive Suite 200, Horsham, 19044, United States

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Organised by
DIA
Contact information
Susan Berkelbach
Horsham, 19044, United States of America
2154426183
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