Good Clinical Practice: ICH-GCP

A unified standard for clinical studies, the Guideline for Good Clinical Practice (GCP) is provided and constantly enhanced by the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). The ICH brings together the health authorities and the pharmaceutical industry from the US, the EU, the non-EU Nordic countries, Japan, Canada, Australia as well as the WHO.

The complete and up-to-date GCP is provided for non commercial purpose by the European Medicines Agency (EMA) at their website:


Last change: 08/26/2014