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CMC: Converting Science in to Regulatory Submission

10 - 11 February 2012, Ahmedabad, India


Introduction
91AV, Manufacturing and Controls (CMC) is one of the three areas that health authorities consider for the review and approval of drug applications. Effective CMC strategies and execution may reduce regulatory burden, enable shorter review times, and support post approval maintenance.

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Venue
Country Inn and Suites By Carlson

Country Inn and Suites By Carlson, Ahmedabad, 380054, India

Organised by
DIA India
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