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 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 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).
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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
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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