Good clinical practice (GCP) is defined as a "standard for the design, conduct, performance, monitoring, auditing, recording, analyzing and reporting of clinical trials." It provides assurance that the obtained data and reported results are credible and accurate. All researchers are obliged to follow the very detailed principles/rules of the International Conference on Harmonization—Good Clinical Practice (GCP). GCP is an international ethical and GCP stands for Good Clinical Practice. GCP is a guide to international ethical and scientific quality standards in clinical trials. The GCP guideline applies to all persons involved in a study. In addition to patient safety, GCP ensures that data and results from clinical trials are valid and reproducible. Goals of the ICH GCP Guideline GCP is the agreed international standard for conducting clinical research. Good Clinical Practice Training is needed for researchers conducting Clinical Trials of Investigational Medicinal Products (CTIMPs). The purpose of this paper is to analyse how compliance with GCP provides protection of the trial subjects and assures quality and credibility of the data obtained. Good Clinical Practice is an international quality standard for conducting trials that involve participation of human subjects. Good Clinical Practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording and reporting that involve the participation of human subjects. .

what is gcp in clinical research