Pharmaceuticals

Draft amendments to the Rules of Good Manufacturing Practice in the Eurasian Economic Union; (158 page(s), in Russian)

Draft Amendments provides for the supplementation of the Rules of Good Manufacturing Practice with Requirements for the production of high-tech medicines harmonized with the current version of the Rules of Good Manufacturing Practice of the European Union and relevant international standards to ensure stable quality of the production process of the specified group of drugs in order to promptly identify deviations in the production process, as a result of which the finished product will be recognized as substandard