Category Archives: CIS regulation

Регистрация медицинских изделий в Таджикистане.

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В настоящее время фармацевтический сектор является одним из приоритетов для развития в Таджикистане. В 2020 г. правительство Таджикистана выпустило постановление «О Государственной программе развития фармацевтической промышленности в Республике Таджикистан на 2021 -2025 годы».  Одной из задач Программы является совершенствование правовой базы Республики Таджикистан в области производства, регистрации, импорта, экспорта и реализации лекарственных средств и медицинских товаров в соответствии с требованиями

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Registration of medical devices in the Republic of Kyrgyzstan.

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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.

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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.

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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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