摘要
分析了医疗器械产品从研发、生产、流通到应用各阶段存在的风险因素,提出了相应的风险防范措施。
Through analyzing the risks of medical devices in their R＆D, production, circulation and use, the author gave some suggestions to strengthen the monitoring and prevention of adverse events due to the medical devices.
出处
《中国医学装备》
2009年第6期21-23,共3页
China Medical Equipment
关键词
医疗器械
不良事件
防范措施
Medical Device
Adverse Event
Preventin
Measure
