eCTD Module 1: FDA, EMA, and Japan Requirements | ICH M4 Guidelines by Peivand Pirouzi, Ph.D

Learn about the organization of the eCTD (Electronic Common Technical Document) Module 1 as outlined by the ICH M4 guidelines. In this video, Professor Peivand Pirouzi, Ph.D., provides an in-depth overview of how Module 1 is structured and aligned with the requirements of regulatory authorities, including the FDA (United States), EMA (European Medicines Agency), and Japan's PMDA (Pharmaceuticals and Medical Devices Agency).

This session will cover:

Key components of Module 1 and their significance.
Regional differences and requirements for the FDA, EMA, and Japan.
Best practices for ensuring compliance and efficiency in eCTD submissions.
Whether you're a regulatory affairs professional or new to eCTD, this video is a valuable resource for understanding the foundation of Module 1.