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Common Technical Document (CTD) for Registration Of Human Drugs SAR  1,380
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Essential of Drug Regulatory Affairs CTD

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Description

OUTLINES

INTRODUCTION to the Common Technical Document (CTD) And ICH

MODULE 1 Administrative and Product Information

MODULE 2 Requirements of the summaries and Overview documents

MODULE 3 Understanding Drug Substance & Drug Products

MODULE 4 Non-Clinical Study Reports

MODULE 5 Clinical Study Reports

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Date

22 October 2023

Location

Online

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