哈萨克斯坦共和国药品注册和医疗器械和医疗设备必须进行国家注册

The list of drugs, IMN and MT subject to state registration

根据哈萨克斯坦共和国药品注册和医疗器械和医疗设备注册的法律要求，根据哈萨克斯坦共和国法典第71条“关于人民健康和医疗保健制度”。

什么哈萨克斯坦共和国药品注册和医疗器械和医疗设备注册机构？

哈萨克斯坦共和国药品注册和医疗器械和医疗设备注册、重新登记和修改，通过“电子政府”门户网站与哈萨克斯坦共和国统一卫生信息系统（SULO）的药物管理系统进行。

State registration and re-registration are subject to manufactured in the Republic of Kazakhstan, as well as imported into its territory drugs, medical devices and medical equipment, including:

药品注册和医疗器械和医疗设备哈萨克斯坦共和国注册产品范围：

1、drugs under the trade names with the indication of the dosage form, dosage, packaging;

2、original medicine;

3、bulk products of medicines, medical products;

4、new combinations of medicines previously registered in the Republic of Kazakhstan with indication of the dosage form, dosage, packaging;

5、medicinal products, previously registered in the Republic of Kazakhstan, but produced by other manufacturers, in other dosage forms, with new dosage, packaging and packaging, other auxiliary substances and the name;

6、medicinal substances not manufactured under good manufacturing practices;

7、drugs of one registration certificate holder produced in different countries at different production sites;

8、medical devices, including diagnostic reagents, contact lenses for vision correction, care products, medical equipment, taking into account their classification depending on the degree of potential risk of medical use;

9、medical devices and medical equipment, previously registered in the Republic of Kazakhstan, but manufactured by other manufacturers;

10、medical devices and medical equipment, previously registered in the Republic of Kazakhstan, but produced in other modifications, with new packaging, a different composition of component parts or a different name;

11、medical devices and medical equipment manufactured by one manufacturer at production sites located (located) in different countries;

12、consumables for medical devices and medical equipment that are medical products, except those specifically designed by the manufacturer for use with a medical product and medical equipment that can function only with this consumable material;

13、medical devices and medical equipment that are part of a specialized vehicle for the provision of medical care;

14、sets (kits) of medical products;

15、laboratory diagnostic devices;

16、medical devices and medical equipment for the prevention, diagnosis, treatment of diseases, assessment of the physiological state of the body, rehabilitation, medical procedures, medical research;

17、medical devices and medical equipment for replacing and modifying parts of tissues, human organs, restoring or compensating for impaired or lost physiological functions;

18、medical devices to control conception.

What document is issued upon completion of the registration procedure for drugs, medical devices and medical equipment? Form RU

1、The state body with a positive decision on registration, re-registration and making changes to the registration dossier of medical devices and medical equipment provides the applicant and expert organization in electronic form