GMP (Good Manufacturing Practice) certification is an internationally recognized standard that ensures that products are manufactured and controlled to the quality required for their intended use. Our site offers articles explaining the main aspects of GMP, the certification process and its importance for pharmaceutical companies.
Learn what procedures and operational processes must be established and maintained in production to meet GMP standards. Learn about the role of GMP in ensuring the safety and effectiveness of medicines and protecting consumers. Learn how pharmaceutical companies undergo GMP compliance audits, including detailed audits of manufacturing processes, quality systems and documentation. Discuss the business benefits of becoming GMP certified, including increased market confidence, improved company image, and increased opportunities to operate in international markets. Get tips on how to prepare for GMP certification, including implementing the necessary quality control processes and training staff.
For the development of the pharmaceutical industry and the export of Ukrainian pharmaceutical products to the European market, recognition of GMP certificates is necessary. This can be done by extending the ACAA agreement between Ukraine and the EU to the pharmaceutical sector
The public discussion on the draft order of the Minister of Health of the Republic of Kazakhstan, which proposes amendments to the order of the Minister of Health of the Republic of Kazakhstan dated October 22, 2020, No. DSM-148/2020, “On the approval of qualification requirements,” has been reopened on the “Open Regulatory Acts” portal.
