The procedure for monitoring the compliance of immunobiological drugs that operate in medical practice, the requirements and international standards, approved by the order of the Ministry of Health of Ukraine from 01.10.2014 № 698 (hereinafter - the Procedure).
In accordance with the Procedure the obligatory laboratory analysis to the indicators of quality specification of quality control methods is subject, in particular vaccines.
Further circulation of a series of immunobiologicals is subject to a positive conclusion on the compliance of immunibiologicals with the requirements of state and international standards.
Information issued by the Region Authorities of the State Service of Ukraine on Medicines and Drugs Control on the quality of administered drugs and Conclusions on compliance of immunobiologicals with the requirements of state and international standards is published on the website of the State Service of Ukraine on Medicines and Drugs Control in the section "State Registers" (https://public-mex.dls2.gov / ResumeResult).
This Procedure does not apply to immunobiologicals imported to Ukraine in accordance with the Law of Ukraine “On Humanitarian Aid”, “On Charitable Activities and Charitable Organization” and “On Implementation of the Global Fund to Fight AIDS, Tuberculosis and Malaria in Ukraine” program, included to the WHO List of pre-qualification and were procured as a result of the procurement procedure conducted by a specialized procurement organization for the implementation of a procurement agreement between the Ministry of Health of Ukraine and the relevant specialized procurement organization.
We provide on quality control of vaccination for influenza prevention, in accordance with the database of the State Service of Ukraine on Medicines and Drugs Control and information received from market authorization holders and/or their representatives, concerning the approximate number of vaccines for the prevention of influenza of the 2021-2022 season for the Ukrainian market.