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Summary of Good Clinical Practice

All NIH-funded clinical investigators and run staff who are involved within the design, conduct, oversight, or management of clinical trials can find out about the necessity to be trained in Good Clinical Practice (GCP).


The principles of fine Clinical Practice (GCP) help assure the protection, integrity, and quality of clinical trials by addressing elements associated with the planning, conduct, and reporting of clinical trials. GCP training describes the responsibilities of investigators, sponsors, monitors, and IRBs within the conduct of clinical trials.

GCP training aims to confirm 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