From August 19 to 22, RK Group LLC The production was successfully inspected by the All-Russian Research and Testing Institute of Medical Equipment (VNIIIMT) of Roszdravnadzor.
Our company has been tested for compliance with the requirements for the implementation, maintenance and evaluation of a quality management system for medical devices, depending on the potential risk of their use.
This is a mandatory procedure related to the registration of medical devices. According to the new rules, from January 1, 2024, registration of new medical devices or changes to previously registered products is impossible without a positive conclusion based on the results of a production inspection.
Grozny plant for the development and production of high-quality medical products LLC "RK Group" showed the efficiency of the quality management system for medical devices in terms of the processes of design and development, production and final control of medical devices, interaction with consumers.
We would like to add that VNIIIMT is a leading organization participating in the formation of ideology and solving state scientific, technical and organizational problems within the framework of a unified technical policy to provide the country's healthcare with medical products.
