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
For more information, please contact us..
Department of Research & Technology Assessment
02-3539734 | researchlerdsin@gmail.com
Lerdsin Hospital Ethics Committee
02-3539733 | lhec.backoffice@gmail.com