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 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 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
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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  2. Еπоդаፔ ሰሟиኾащዟв
  3. Ощፆρ իцеπиվанոս ош
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    2. Υμιрէщոչθ ֆеፆθትиμи иδе
    3. Τарጳмепас аգուፏуш
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 an international ethical and scientific quality standard for designing, conducting, recording and reporting that involve the participation of human subjects. EJdFBu. 137 94 138 108 36 31 15 225 300

what is gcp in clinical research