Tag 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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State registration of medical devices in the Republic of Belarus.

As you know, in the near future, namely from January 1, 2022, the five countries of the Eurasian Economic Union will be united by one harmonized procedure for registration of medical devices. However, most countries of the Union have their own national registration procedures. How is the state registration of MD organized in these countries? What are its features for

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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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