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 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. Good clinical practice ( GCP) is a set of internationally-recognised ethical and scientific quality requirements that must be followed when designing, conducting, recording and reporting 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). 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. The Good Clinical Laboratory Practices (GCLP) concept possesses a unique quality, as it embraces both the research and the clinical aspects of GLP. The development of GCLP standards encompasses applicable portions of 21 CFR parts 58 (GLP) and 42 CFR part 493 (Clinical Laboratory Improvement Amendments -CLIA) . sW5b5.

what is gcp in clinical research