Practical Approach to Creating Clinical Study Reports from Data Collection to Final Approval
This course will provide an in-depth analysis of the preparation of a clinical overview for pharmaceutical products (drugs and biologics) in accordance with ICH guidelines concerning development of Module 2.5 of a Common Technical Document (CTD).
This course will provide an in-depth analysis of the preparation of a clinical overview for pharmaceutical products (drugs and biologics) in accordance with ICH guidelines concerning development of Module 2.5 of a Common Technical Document (CTD).
