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The Department of the Good Practices Inspectorate (GxP) of the State Unitary Enterprise "Center for Good Practices" operates on the basis of the Resolution of the Cabinet of Ministers of the Republic of Uzbekistan dated September 18, 2019 No. 788 "On additional measures to introduce the requirements of Good Practices (GxP) in the pharmaceutical industry."
The Inspectorate of good practices (GxP) department performs the following functions:
- Carrying out pharmaceutical inspections of domestic pharmaceutical enterprises and organizations for compliance with the requirements of Good Practices (GxP);
-Periodic on-site inspection of domestic pharmaceutical companies and organizations to confirm compliance with the requirements of the Standards of Good Practice (GxP) during the validity of the issued certificate;
- In the process of state registration of medicines in the Republic of Uzbekistan, pharmaceutical inspections are carried out with a visit to the site of foreign pharmaceutical companies for compliance with the requirements
"Good Manufacturing Practice (GMP)" and, in accordance with the established procedure, issuance of an opinion based on the results of the inspection.