美国定制类医疗器械监管模式介绍与思考

      Study of Regulatory Requirements of Customized Device in the U.S.

      • 摘要: 该文主要介绍了美国定制类医疗器械的监管模式和现状,同时梳理了人道主义用器械、3D打印器械的监管要求,进一步对比了定制类器械与人道主义用器械的异同,为建立我国定制类医疗器械法规体系提供参考。

         

        Abstract: This article introduces the regulatory requirements of customized device in the U.S. And it also proposes suggestion and reference through comparative study on relationship among customized device, humanitarian use device and 3D printing device, and on similarities and differences of American regulatory requirements between customized device, and humanitarian used device.

         

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