节点文献

广东省药品监督管理局深入推进医疗器械监管综合改革助力医疗器械创新发展

Guangdong Medical Products Administration Further Promotes the Comprehensive Reform of Medical Device Regulation to Facilitate Its Innovative Development

  • 推荐 CAJ下载
  • PDF下载
  • 不支持迅雷等下载工具,请取消加速工具后下载。

【作者】 苏盛锋邱楠张锋

【Author】 SU Sheng-feng;QIU Nan;ZHANG Feng;Guangdong Medical Products Administration;

【机构】 广东省药品监督管理局

【摘要】 广东省是全国医疗器械产业重要集聚区。随着粤港澳大湾区、深圳先行示范区两大国家战略相继实施,广东省药品监督管理局着力推进医疗器械监管现代化综合改革。在顶层设计上,出台鼓励政策、参与产业规划;在创新服务上,加强申报交流,提升服务项目能力,并取得了一定的成效。未来广东省药品监督管理局还将在夯实技术支撑、强化研究协同、吸引研究团队、推动临床应用、建设临床研究基地等领域继续进行创新探索,促进广东省医疗器械产业持续创新和高质量发展。

【Abstract】 Guangdong is one of the most important medical device industry clusters in China. With the successive implementation of the national strategy of Guangdong–Hong Kong–Macao Greater Bay Area and Shenzhen Pioneering Demonstration Zone, Guangdong Medical Products Administration(GDMPA) substantially promotes the comprehensive reform of the modernization of medical device administration. In terms of top-level design, GDMPA introduces encouragement policies and participates in industry planing. In terms of service innovation, GDMPA continuously upgrades high-quality resources,improves project service capacities and enhances application exchanges, gaining some achievements. In the coming future,GMPA will commit to series of innovative explorations on strengthening technical support, enhancing research collaboration,attracting research and development team, pushing clinical applications, constructing clinical centers, which will boost sustainable high-quality development of Guangdong medical device industry.

  • 【文献出处】 中国食品药品监管 ,China Food & Drug Administration Magazine , 编辑部邮箱 ,2022年12期
  • 【分类号】F426.4;F203
  • 【下载频次】23
节点文献中: 

本文链接的文献网络图示:

本文的引文网络