1.
Analysis of 239 Reports of Medical Device Adverse Events;
239例医疗器械不良事件报告分析
2.
Analysis of 415 doubted reports on adverse medical device event;
415例可疑医疗器械不良事件报告分析
3.
Analysis of 324 doubted reports on adverse medical device event;
324例可疑医疗器械不良事件报告分析
4.
Analysis of 3123 Reports on Suspected Medical Device Adverse Event
3123例可疑医疗器械不良事件报告分析
5.
Discussing the Influence Factors on Reporting Medical Device Adverse Event in China;
我国医疗器械不良事件报告的影响因素探讨
6.
Analysis of the Medical Device Adverse Events Reports in 2007 in Guangdong Province;
广东省2007年可疑医疗器械不良事件报告分析与思考
7.
Research on Gray Dynamic GM(1,1) Forecasting Model for MDRs′ Quantity;
基于灰色动态GM(1,1)的医疗器械不良事件报告数量预测模型研究
8.
The Enlightenment for Our Country from the UK 2008 Annual Report of Medical Device Adverse Event
英国2008年度医疗器械不良事件报告对我国的启示
9.
Discussion and Report on the Medical Device Adverse Event of Orthopedic Implants;
浅议骨科植入性医疗器械不良事件及其报告工作
10.
Adverse Event Reporting Guidance for the MedicalDevice Manufacturer or its Authorized Representative;
医疗器械制造商或其授权代理商的不良事件报告指南
11.
Study on Training Needs for Survey of Adverse Effects of Medical Devices;
医疗器械不良事件监测培训需求研究
12.
Study on the Current Situation of Medical Device Adverse Events Monitoring in China;
我国医疗器械不良事件监测现状研究
13.
Medical Devices Adverse Events Monitoring ?the Present and the Future;
医疗器械不良事件监测-现状与展望
14.
A New Subject For the Postmarket Surveitlance of Medical Devices-Medical Device Advers Event Reporting;
医疗器械监督管理的新课题——医疗器械不良事件监测
15.
The Effect of Medical Device Adverse Event Monitoring on Pre-market Medical Device Administrative Examination
浅谈医疗器械不良事件监测对医疗器械上市前行政审批的作用
16.
Investigation of Medical Device Adverse Events Monitoring in Shandong Province;
山东省医疗器械不良事件监测工作调查分析
17.
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
18.
The Thought of Medical Device Adverse Event Monitoring in Xinjiang Uygur Autonomous Region
新疆地区医疗器械不良事件监测工作的思考