1.
Discussions on the Regulatory Requirements for Medical Device Risk Management in China
谈我国医疗器械风险管理的法规要求
2.
The Present situation and thinking of Risk Management for Medical Devices in Use in Modern Hospital
现代医院在用医疗器械风险管理的现状与思考
3.
Problems and Countermeasures of the Application of Risk Management to Medical Devices in Hospitals;
在用医疗器械风险管理问题及对策研究
4.
Biological Evaluation within a Risk Management Process;
在医疗器械风险管理体系中的生物学评价
5.
Review on Application of Risk Management to Medical Devices in Hospitals;
国内外在用医疗器械风险管理问题初探
6.
Discussion on the Role of Clinical Engineers in Medical Device Risk Management and Their Developments
浅谈临床工程师在医疗器械风险管理中的作用及队伍建设的建议
7.
Thoughts on the Developing Post-market Medical Device Risk Management System in Primary Monitoring Organization;
基层完善医疗器械上市后风险管理体系的思考
8.
Analysis on the Medical Device Administration Events Monitoring and Risk Management in China from "Extracorporeal Circulation Set Tube Event"
从“珠海体外循环管道事件”看我国医疗器械不事件监测与风险管理
9.
Analysis of the Optimizing Approach of Institution in Medical Device Adverse Event Monitoring Based on Risk Management
基于风险管理的我国医疗器械不良事件监测政策优化理论分析
10.
Analysis and Apocalypse of FDA Risk Management of Post-Market Medical Device;
浅析美国医疗器械上市后风险管理模式及对我国的启示
11.
The Research on Logistics Management of Medical Device in One Hospital in Shanghai
上海市某医院医疗器械物流管理研究
12.
Introduction and Application Prospect of Risk Analysis Methods for Medical Devices;
医疗器械风险分析方法的介绍与应用展望
13.
Risk Cause and Countermeasure on Adverse Apparatus Events of Medical Institutions
医疗机构器械不良事件风险成因及对策
14.
Comprehending the System for ISO13485 Medical Apparatus Quality Managment
理解ISO13485医疗器械质量管理的体系
15.
The Moral Hazard and Guard in the Social Medical Insurance of Our Country;
我国社会医疗保险中的道德风险管理
16.
Study on the Risk Management Problem of Social Medical Insurance Fund in China;
我国社会医疗保险基金风险管理问题
17.
Better Medical Devices Regulations for Better Health Care: Enlightenment for Medical Devices Regulatory Reform in China, from Experiences of the EU and the USA;
欧美医疗器械管理经验及对中国医疗器械法规体系改革的启示
18.
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