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).
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) .
Good Clinical Research Practice (GCP) is a process that incorporates established ethical and scientifi c quality standards for the design, conduct, recording and reporting of clinical research involving the participation of human subjects. Compliance with GCP provides public assurance that the rights, safety, and well-being of research
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what is gcp in clinical research