摘要
医疗器械产业发展越来越快,新的医疗器械在批准用于公共健康的程序之前,必须要对它的质量、功效、可靠性和安全性进行临床试验。我院根据自身科室特点,利用我院医疗资源开展医疗器械临床观察。积累了一些经验,总结出来,供大家参考。
The development of medical instruments industry becomes more and more rapid.Before new medical devices been approved of using publicly,it is necessary to take clinical trials to the quality, effectiveness,reliability and safety of medical instruments. According to the characteristics of our hospital,we took some clinical observation of medical instruments,and this paper introduces the experience of our hospital.
出处
《中国医疗设备》
2010年第1期73-74,82,共3页
China Medical Devices
关键词
医疗器械
临床观察
医疗器械不良事件
medical instruments clinical observation medical instruments adverse event
