Roles and Responsibilities Under ICH GCP


Lesson Code: CTM-801


  • Category: Clinical Trials GCP - Intermediate

Description

Describes the roles and responsibilities of the different parties involved in initiating, conducting, and overseeing clinical trials according to ICH Good Clinical Practice. After explaining the need for ICH GCP, the module describes the part played by sponsors, investigators and IRB/IEC. The roles of other key contributors to the clinical trial process are also described.