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.

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.
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    • what is gcp in clinical research