Explanation of the requirements of regulatory legal acts in the field of circulation of medicinal substances and medical products (hereinafter - DZ and MB).

11.06.2025. The Department of the Medical and Pharmaceutical Control Committee of the Ministry of Health of the Republic of Kazakhstan for Aktobe region (hereinafter - the Department) with the heads and representatives of medical organizations related to the issues of regulatory legal acts in the field of DZ and MB circulation, including the introduction of the GPP standard of appropriate pharmacy practice (hereinafter - GPP Standard), pharmacological supervision and monitoring of the side effects of DZ and MB, writing prescriptions for drugs, compliance with the rules of retail sales an explanation was given at the seminar-council.

Also, during the seminar, it was reported that administrative liability was considered in case of non-compliance with the requirements of the regulatory legal acts in the field of DZ and MB.

Representatives of medical organizations that implemented the GPP standard shared their experience of implementing the GPP standard.          

Source : https://www.gov.kz/memleket/entities/dkmfk-aktobe/press/news/details/1017652?lang=kk