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引用次数: 0

摘要

欧亚经济联盟框架内的医疗器械市场由专门立法监管,确保形成共同市场,产品符合所有必要条件。这就保证了医疗设备和物品的高质量,有助于提高医疗过程的安全性和效率。根据国际惯例制定统一的要求是重要的一步,因为这不仅能保证单个国家的高标准,还能保证整个欧盟的高标准。这种方法有助于增强欧亚经济联盟各国制造商对医疗产品的信心。文章对规范欧亚经济联盟框架内医疗设备和物品共同市场的形成与运行问题的法律基础进行了研究。文章分析了俄罗斯联邦在医疗用品市场方面的规范性法律基础。此外,还分析了俄罗斯联邦在医疗器械市场相关问题方面的监管框架。根据研究结果得出了相应结论。
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[The issues of development and functioning of common market of medical equipment and articles within the framework of the Eurasian Economic Union].

The market of medical devices within the framework of the Eurasian Economic Union is regulated by special legislation that ensures formation of common market and compliance of products with all necessary requirements. This allows to ensure high level of quality of medical equipment and articles that contributes into improving safety and efficiency of medical procedures. The development of uniform requirements, considering world practices, is an important step, since it allows to guarantee high standards not only at level of single states, but also at level of the entire Union. This approach facilitates reinforcement of confidence to medical production of manufacturers from he Eurasian Economic Union countries. The article examines normative legal base regulating issues of formation and functioning of common market of medical equipment and articles within the framework of the Eurasian Economic Union. The analysis of normative legal base of the Russian Federation in section related to medical articles market was carried out. The analysis of the regulatory framework of the Russian Federation in terms of issues related to the market of medical devices was also carried out. The corresponding conclusions were made based on the study results.

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