Good Clinical Practice designates set up rules for the execution of medical treatments or clinical tests, dependent on the current conditions of the scientific realization, on the basis of ethical and practical criteria.

These are supplemented by guidelines for the production of the assigned medicaments and the medicine products (GMP Good Manufacturing Practice) as well as the achievements of the laboratory medicine (GLP Good Laboratory Practice needed in the context of the study).

Organizations, which sketch such rule sets, are internationally international in Europe the European medicament agency (EMEA) and the Conference on Harmonisation OF Technical requirement for Registration OF Pharmaceuticals for human Use (I).

Related links

• Pdf with GCP guidelines (English)

Articles in category "Good Clinical Practice"

We found here 8 articles.

Related Websites

We found here 5 related websites.

• Clinical Trials--Information for Health Professionals
  Good Clinical Practice in FDA-Regulated Clinical Trials. ... Good Clinical Practice (GCP) is a standard for the design, conduct, performance, monitoring, ...


• E 6 (R1) Guideline for Good Clinical Practice
  Good Clinical Practice (GCP) is an international ethical and scientific quality ... Adherence to all the trial-related requirements, Good Clinical Practice ...


• Guidance for Industry
  Good clinical practice (GCP) is an international ethical and scientific quality ... 1.24 Good Clinical Practice (GCP): A standard for the design, conduct, ...


• ICH
  The official website of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). ...


• MRC Guidelines for good clinical practice in clinical trials
  Conference on Harmonisation