1.
Discussion on the Several Legal Issues in Supervision of Medical Device;
试论医疗器械监管中的几个法律问题
2.
Research on Challenges and Solution of Jilin Province's Medical Device Regulation
吉林省医疗器械监管问题及对策研究
3.
By Our Country Medical Instrument Supervising and Managing Legal Flaw and Countermeasure;
论我国医疗器械监管的法律缺失与对策
4.
Thinking on the Reform of Chinese Medical Device Regulatory System;
我国医疗器械监管法规体系建设之思考
5.
A Brief Summary of the Work Done in Carrying out 《the Administrative Permission Law》 by the Supervision Departments for Medical Devices;
医疗器械监管部门贯彻“行政许可法”的工作小结
6.
Supervision and Administration for Medical Devices when Facing a Sudden Public Health Event;
面对“突发公共卫生事件”的医疗器械监管
7.
Review on the Scientific Supervise and Management of Medical Device through the Subject Characteristic of the Medical Device
从医疗器械的学科特点看医疗器械的科学监管
8.
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
9.
Discussion on regulating drug and medical instrument advertisement on the internet;
网络药品、医疗器械广告监管工作初探
10.
The Comparison of the Regulations of Medical Device Clinical Trials between China and U. S.
中美医疗器械临床试验监管比较分析
11.
Discussion of the Medical Device Clinical Research and Supervision
医疗器械临床研究方式和监管的探讨
12.
The Comparison and References of the Medical Device Manufacturers’ Supervision and Management Between the USA and China;
中美医疗器械生产企业监督管理之比较与借鉴
13.
The Comparison Study of American and Chinese Regulatory System of Clinical Laboratory Medical Device;
中美临检类医疗器械产品监管比较研究
14.
Analyses about the Optimizing Approach of Supervising Medical Device Market Institution;
医疗器械市场监管制度的优化途径分析
15.
Exploration on the Regulation Mode of Medical Device Quality and Safety on a Life-Circle Basis;
医疗器械的全寿命质量与安全监管模式探讨
16.
Study on the Problem and Countermeasures of Medical Device Manufacturing Industry Regulation
医疗器械生产行业监管存在问题及对策研究
17.
Examples of Preparation and Supervision of Sterile Medical Instrument Used Water
无菌医疗器械生产用水制备及监管实例
18.
Concerned about the Marketing of Medical Equipment by the Method of Personal Experience
重视对体验式销售医疗器械营销模式的监管