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Medical Devices, Pharmaceuticals

ICH GCP Obligations of Investigators Conducting Clinical Trials

About the Course

This online course addresses the obligations of investigators as described by the International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). The compliance training focuses on the investigator’s responsibilities to protect the rights and welfare of human subjects and ensure data integrity. By extension, these responsibilities also apply to other investigation site staff involved in the planning, conduct, recording, and reporting of clinical trials.