Introduction of GMP standards discussed at conference in Moscow
18.09.2025
Achievements and development prospects of the pharmaceutical industry within the Eurasian Economic Union were discussed in Moscow at the 10th All-Russian GMP Conference featuring Chinara Mambetalieva, Deputy Director of the Eurasian Economic Commission's Technical Regulation and Accreditation Department.
During the discussion the EEC representative noted an important role of introducing GMP standards into pharmaceutical manufacturing.
"Compliance with GMP guidelines defines quality, efficacy and safety of medicines; hence, public health," mentioned Chinara Mambetalieva. "The introduction of unified regulations in this field has significantly improved the quality of medicines, as well as qualifications, training and certification of staff at pharmaceutical plants."
Chinara Mambetalieva also attended the session "The Common Market of Medicines for Human Use in the EAEU" that considered industry-specific issues including those related to regulatory interaction in the pharmaceutical field.
GMP (Good Manufacturing Practice) is a system of international regulations and guidelines setting requirements for production and quality control to guarantee safety and efficacy of products including pharmaceuticals.