This course is designed to advance your understanding of the importance and underlying principles for CMC requirements from the regulatory perspective.
Participants will gain an understanding of the CMC portion of a Common Technical Document (CTD) which is the format that regulatory submissions in Canada and the EU must be filed.
Who Should Attend?
This course is designed for:
Directors Managers, Supervisors, Associates in the Pharmaceutical, Biopharmaceutical, Vitamins, Herbals, Medical Devices, and more.
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