摘要
该文围绕在用医疗器械产品质量监管所亟需明确的生命周期、监管边界、监管对象、监管重点、监管依据、执行标准等问题逐一分析,并提出明确且开创性的学术主张,为在用医疗器械产品质量监管做出有益的理论探索。
This paper focuses on issues needed to be clear towards the product quality supervision of medical devices in use. The life circle of medical devices, the supervision regarding its boundary, target, emphasis, basis and standards have been analyzed in turn. A clear and creative idea is also provided for theoretical exploration of the supervision on medical devices in use.
出处
《中国医疗器械杂志》
CAS
2014年第3期207-209,共3页
Chinese Journal of Medical Instrumentation
关键词
在用医疗器械
质量
监管
medical devices in use, quality, supervision