摘要
本文介绍了我国在用医疗器械的质量现状,分析了在用医疗器械监管的新形势,并对全面开展在用医疗器械监管可能面临的问题和困难进行了深入思考,最后对如何保障在用医疗器械监管的顺利开展提出了几点建议。
In this paper, the current quality situation and new supervision situation of in-use medical devices in China is introduced. Based on the deep pondering over the problems and difficulties in comprehensive supervision of in-use medical devices, some suggestions are put forward to ensure that the supervision can run smoothly.
出处
《中国医疗设备》
2015年第1期68-70,共3页
China Medical Devices
关键词
医疗器械监管
计量指标
强制检测
在用医疗器械
medical device supervision
measuring index
mandatory testing
in-use medical device
