Category Archives: CIS regulation

Registration of medical devices in Tajikistan.

Currently, the pharmaceutical sector is one of the priorities for development in Tajikistan. In 2020, the government of Tajikistan issued a resolution “On the State Program for the Development of the Pharmaceutical Industry in the Republic of Tajikistan for 2021-2025”.  One of the objectives of the Program is to improve the legal framework of the Republic of Tajikistan in the

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Registration of medical devices in the Republic of Kyrgyzstan.

The Kyrgyz Republic, along with Kazakhstan, Belarus, Armenia and Russia, is part of the Eurasian Economic Union, which means that from 01.01.2022 on the territory of this country the rules for registration of medical devices defined by the legislation of the EAEU will come into force. However, unlike, for example, Armenia, Kyrgyzstan has a national registration system for medical devices,

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Registration of medical devices in Uzbekistan.

The main legislative act regulating the procedure for state registration of medical devices is Resolution No. 213 dated March 23, 2018 “Regulations on the procedure for state registration of medical devices medicines, medical products and medical equipment and the issuance of a registration certificate.” According to this Resolution, medical devices in Uzbekistan are divided into two groups: medical devices (MD)

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The market of medical devices in Uzbekistan.

The market of medical devices is an actively developing part of the pharmaceutical sector of the Uzbek economy. Despite the fact that import still plays an important role and account for about 80 % of the pharmaceutical and medical market, currently some benefits are provided to local manufacturers for the development of the pharmaceutical industry in Uzbekistan: medical devices and

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