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Good clinical practice

Good clinical practice (GCP) is an international quality standard that is provided by ICH, an international body that defines standards, which governments can transpose into regulations for clinical trials involving human subjects. A similar guideline for clinical trials of medical devices is the international standard ISO 14155, that is valid in the European Union as a harmonized standard. These standards for clinical trials are sometimes referred to as ICH-GCP or ISO-GCP to differentiate between the two and the lowest grade of recommendation in clinical guidelines.[1]

GCP follows the International Conference on Harmonisation (ICH) of GCP guidelines. GCP enforces tight guidelines on ethical aspects of a clinical study. High standards are required in terms of comprehensive documentation for the clinical protocol, record keeping, training, and facilities, including computers and software. Quality assurance and inspections ensure that these standards are achieved. GCP aims to ensure that the studies are scientifically authentic and that the clinical properties of the investigational product are properly documented. Ongoing research shows that whether conducting research involving a new drug, a behavioral intervention, or an interview or survey, GCP provides investigators and their study teams with the tools to protect human subjects and collect quality data.[2][3]

GCP guidelines include protection of human rights for the subjects and volunteers in a clinical trial. It also provides assurance of the safety and efficacy of the newly developed compounds.

GCP guidelines include standards on how clinical trials should be conducted, define the roles and responsibilities of clinical trial sponsors, clinical research investigators, and monitors. In the pharmaceutical industry monitors are often called Clinical Research Associates.

ICH GCP overview


GCP has been called 'a less morally authoritative document' than the Declaration of Helsinki, lacking moral principles and guidance in the following areas:[4]

  • Disclosure of conflict of interest
  • Public disclosure of study design
  • Benefit for populations in which research is conducted
  • Reporting of accurate results and publication of negative findings
  • Access to treatment after research has been conducted
  • Restriction of use of placebo in control group where effective alternative treatment is available

See also


  • Verma K (2013) Base of a Research: Good Clinical Practice in Clinical Trials. J Clin Trials 3: 128. doi:10.4172/2167-0870.1000128


  1. ^ Examples of clinical practice guidelines using 'good clinical practice' as lowest grade of recommendation
  2. ^ Verma K (2013) Base of a Research: Good Clinical Practice in Clinical Trials. J Clin Trials 3: 128. doi:10.4172/2167-0870.1000128
  3. ^ "Base of a Research: Good Clinical Practice in Clinical Trials | Full-text OMICS Publishing Group". Retrieved 2013-11-23. 
  4. ^ doi:10.1016/S0140-6736(08)61936-4, retrieved at on 10 Aug 2014

External links