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 Abstract. This chapter looks at the purpose and history of the development of good clinical practice (GCP). The international conference on harmonisation (ICH) GCP is the international quality standard for conducting clinical research to ensure the rights and well-being of patients are protected and the resulting data are valid. 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. 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 an international ethical and scientific quality standard for designing, conducting, recording and reporting that involve the participation of human subjects. 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. 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). EdCgqe.

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