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24.09.2025
EURASIAN ECONOMIC COMMISSION (EEC) COUNCIL UPDATED THE EAEU GOOD CLINICAL PRACTICE (GCP) RULES
The GCP rules have been revised. The document was prepared based on the ICH GCP (Good Clinical Practice Guidelines), that is document E6 (R2) of the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use. 
These rules must be followed in all drug trials, the data from which are submitted to authorised bodies (expert organisations) of member states. The principles they establish also apply to other clinical trials that may impact the safety and well-being of human subjects.

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