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The examination of quality, efficiency safety of medical products is part of the procedure for state registration of medicines. The inspection is carried out basing on the analysis of the submitted information about the production, the documents for assessing the accordance of medical products according to classification depending on the potential risk of their use.
The examination of quality, efficiency and safety of medical products in the FBGU Center of Monitoring and Clinical and Economic Inspection is carried out by the Department of Expertise of Quality, Efficiency and Safety of Medical Devices and the Department of Expertise and Monitoring of Safety of Medical Devices.
The information-analytical and expert support for activities to monitor compliance with the quality and safety of medical activities is the activity of the FBGU Center of Monitoring and Clinical and Economic Inspections, which is carried out on the basis of the State order for the current year, to promote control in the sphere of health protection by authorized state authorities in accordance with the current legislation.
Information-analytical and expert support is provided by the Training and Methodological Department of the FBGU Center of Monitoring and Clinical and Economic Expertise.
Video "On the Procedure for the preparation of documents for the purpose of"
Video "Gos. Registration of medical devices"
In this paper, which was attended by more than 500 experts from 59 regions of the countryСписок