1) adverse apparatus events of medical institutions
医疗机构器械不良事件
1.
Methods Through the analysis risk cause on adverse apparatus events of medical institutions, the major factors of causing the medical institutions adverse apparatus events and the ways of solving the problems were found.
目的:分析医疗机构器械不良事件的风险成因,以期引起医疗机构的重视,减少医疗器械不良事件的发生。
2) MDRS
医疗器械不良事件报表
3) Medical Device Administration Events(MDAE)
医疗器械不良事件
1.
An international platform for Medical Device Administration Events(MDAE)Information Exchange was introduced in this article.
通过介绍国际医疗器械法规协调组织发起的,在国际范围内交换医疗器械不良事件监测信息的国家医疗器械管理机构报告,旨在为我国开展医疗器械不良事件监测信息管理及参与国际信息交流提供借鉴。
2.
Objective By analyzing the Medical Device Administration Events(MDAE) reports of Guangdong Province in 2007,to provide references for monitoring work.
目的通过对广东省2007年接收的可疑医疗器械不良事件报告表进行统计分析,为进一步开展监测工作提供参考。
3.
Objective To investigate the knowledge level related to Medical Device Administration Events(MDAE) among healthcare professionals.
目的了解北京市医疗机构医务人员对医疗器械不良事件及相关监测工作的知晓程度,为深入开展医疗器械不良事件监测奠定基础。
4) medical devices vigilance
医疗器械不良事件监测
1.
Methodology probing in medical devices vigilance——Failure Mode Effects and Criticality Analysis;
医疗器械不良事件监测方法学的探讨——故障模式影响及危害性分析
5) adverse events of medical device
医疗器械不良事件
1.
Statistic analysis of adverse events of medical device reports in 2006 in Hunan province;
湖南省2006年可疑医疗器械不良事件报告分析
2.
Statistic analysis of adverse events of medical device reports in 2007 in Anhui Prorince;
安徽省2007年可疑医疗器械不良事件报告分析
6) Medical device adverse event
医疗器械不良事件
1.
Comment about Medical Device Adverse Event Vigilance& Evaluation Related Regulations;
医疗器械不良事件监测和再评价相关法规解读
2.
The reporting of medical device adverse event(MDAE) is the first step on the detection of medical device problems and taking risk management actions.
医疗器械不良事件报告是发现医疗器械安全性隐患和采取风险管理措施的前提。
补充资料：医疗
1.医治。 2.疾病的治疗。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条