This document discusses ICH-GCP and compares it to Indian GCP guidelines. It begins by explaining that ICH is an international body that establishes quality standards for clinical trials called Good Clinical Practice (GCP). GCP guidelines ensure clinical trials are scientifically valid and investigational products are properly documented. The document then outlines some key differences between ICH-GCP and Indian GCP guidelines, such as investigator qualifications, informed consent procedures, and the roles of investigators, monitors and ethics committees.