ICH Good Clinical Practice (GCP) Training R3

Content reflects ICH GCP E6 (R3)

The principles of Good Clinical Practice (GCP) help assure the safety, integrity, and quality of clinical trials by addressing elements related to the design, conduct, and reporting of clinical trials. GCP training describes the responsibilities of investigators, sponsors, monitors, and IRBs in the conduct of clinical trials. 

GCP training aims to ensure that:

• the rights, safety, and well-being of human subjects are protected
• clinical trials are conducted in accordance with approved plans with rigor and integrity
• data derived from clinical trials are reliable

View each video to learn more about different topics in GCP.  To pass this course, you must complete the assessment with a score of 80% or greater.