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[Reference and Innovation: Research on the Construction of Medical Device Registrar System].

作者信息

Xu Lai, Lin Senyong, Hu Lijun, Yang Yihan, Wu Zhong, Huang Jing, Jiang Haihong

机构信息

Shanghai Food and Drug Administration, Shanghai, 200003.

Institute of Science and Technology Information, SHFDA, Shanghai, 200233.

出版信息

Zhongguo Yi Liao Qi Xie Za Zhi. 2019 May 30;43(3):192-196. doi: 10.3969/j.issn.1671-7104.2019.03.010.

Abstract

In order to strengthen the integration of reform system and build a comprehensive integration of openness and innovation, the medical device registrar system has become the institutional choice to promote the reform of the medical approval system and the innovation and development of the industry. The system allows scientific researchers, R&D institutions and enterprises to become applicants for medical device registration and to consign the production of samples and products, thus realizing the separation of market license and production license, and breaking the binding relationship between registration and production in current regulations. The medical device registrar system has laid a theoretical foundation for remolding the management system of medical devices, and has also made practical exploration for improving the reform of the medical devices supervision system, so it has important theoretical and practical significance.

摘要

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