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Guidance Documents/Guidance-Document/M4 Organization of the Common Technical Document for the Registration of Pharmaceuticals for Human Use Guidance for Industry

M4 Organization of the Common Technical Document for the Registration of Pharmaceuticals for Human Use Guidance for Industry

Detailed guidance document from FDA and regulatory agencies.

Document Details

Guidance Document

October 3, 2017

April 24, 2020

Center for Drug Evaluation and Research

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