摘要
本文对植入性医疗器械不良事件的产生原因分析,指出植入性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,提出相应的防范措施。
Through analyzing the risks products in research and development, production, circulation and use of implants medical devices, And makes some suggestions to strengthen the monitoring and preventing measures of adverse events for the medical devices.
出处
《解放军医院管理杂志》
2012年第3期220-221,共2页
Hospital Administration Journal of Chinese People's Liberation Army
关键词
植入性医疗器械
不良事件
防范措施
implanting medical device
adverse events
preventive measures
