Uutiset-näyttösivun murupolku en
Good Clinical Practice (GCP) guideline is now available in Finnish
The latest R3 version of the European Medicines Agency’s ICH E6 guideline entered into force in the EU about a year ago. A working group coordinated by Fimea has completed an unofficial Finnish translation of the guideline, which is now accessible on the Fimea website.
The translation is aimed especially at academic researchers and people who are not familiar with clinical trials or are just starting to work in the field.
The aim of the translation project was to produce a clear, easy-to-understand and accessible Finnish translation of the updated GCP guideline. The working group paid particular attention to language-specific nuances and the terminology introduced with the latest update of the guideline.
The ICH Good Clinical Practice (GCP) guideline is an international standard for the design, conduct, documentation and reporting of clinical trials involving human subjects.
Good Clinical Practice (GCP) (GCP) ICH E6 (R3)
Unofficial Finnish translation, version 1, July 2026 (pdf, fimea.fi)
Guideline of the European Medicines Agency (EMA) ICH E6 (R3) (in English, ema.europa.eu)