In accordance with the Code of the Republic of Kazakhstan on Citizens' Health, the main purpose of the procedure is to establish the safety of medical devices for human health.

Medical equipment, apparatus, complexes, consumables, monitoring devices, devices and instruments, reagents, calibrators, control materials and other products used for medical purposes separately or in combination with each other and cannot be presented on the market and included in the register, if their quality, efficiency and safety are not confirmed during state registration.

Registration of medical devices (hereinafter - MD) in Kazakhstan is one of the work profiles of the GO PHARM group of companies, which is one of the leaders in the field of registration among international consulting companies.

Benefits of cooperation with professionals

The staff of the GO PHARM company will assist in the registration of medical devices. These are 83 specialists who work in various areas of regulatory activity.

We approach each project individually and guarantee confidentiality.

Medical devices (MD) subject to state registration

• Equipment used for prevention, treatment, rehabilitation.
• Apparatus for the study of health.
• Consumables, accessories for equipment and apparatus.
• Devices for health monitoring and self-control (eg blood pressure monitors, glucometers).
• Instruments, devices that are used to change the physiological functions of the body or restore them.
• Medical devices materials, products, solutions, reagents, kits, kits used to provide medical care.