EUROPEAN COMMISSION
DG Internal Market, Industry, Entrepreneurship and SMEs
太原英语Consumer, Environmental and Health Technologies
Health technology and Cosmetics
备注：中文翻译中的临床调查=临床研究，评估=评价、设备=器械、数据=资料
MEDDEV 2.7/1 revision 4 2016红白歌会
连杆总成>法文翻译在线
June 2016
GUIDELINES ON MEDICAL DEVICES 医疗器械指南
CLINICAL EVALUATION:
A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES UNDER DIRECTIVES 93/42/EEC and 90/385/EEC
Note
The prent Guidelines are part of a t of Guidelines relating to questions of application of EC-Directives on medical Devices. They are legally not binding. The Guidelines have been carefully drafted through a process of intensive consultation of the various interested parties (competent authorities, Commission rvices, industries, other interested parties) during which intermediate drafts where circulated and comments were taken up in the document. Therefore, this document reflects positions taken by reprentatives of interest parties in the medical devices ctor. The guidelines incorporate changes introduced by Directive 2007/47/EC amending Council Directive 90/385/EEC and Council Directive
93/42/EEC.
本指南为一系列与CE—医疗器械指令应用问题相关的指南中的一部分。并不具有法律约束力。该指南在经过与各个利益方（主管当局、服务委员会、行业委员会、其他利益相关团体）进行深入协商之后谨慎拟定而成，期间对中期草案进行了传阅，而且部分意见还为本
文件所采纳。因此，本文件反映出了来自医疗器械行业的利益团体代表所持的立场。本指南包含了指令 2007/47/EC对90/385/EEC和 93/42/EEC修正中的变更
（没规定实施时间）
MEDICAL DEVICES DIRECTIVES CLINICAL INVESTIGATION
somuch
美国大学雅思CLINICAL EVALUATION:
A GUIDE FOR MANUFACTURERS AND NOTIFIED BODIES UNDER DIRECTIVES 93/42/EEC and 90/385/EEC
Index
1. 4
2. Scope ............................................................................................................................... 4
3. References ......................................................................................................................... 4
职称英语考试资料4. . 5
5. 8
6. General principles of clinical evaluation ............................................................................. 9
6.1. What is clinical evaluation? ................................................................................................ 9
6.2. When is clinical evaluation undertaken and why is it important?...................................... 10
hopkins6.2.1. Clinical evaluation undertaken for the development of a medical device ......................... 10
6.2.2. Clinical evaluation for initial CE-marking .......................................................................... 11
6.2.3. Updating the clinical evaluation ........................................................................................ 11
6.3. How is a clinical evaluation performed? ........................................................................... 13
insky
6.4. Who should perform the clinical evaluation? .................................................................... 14
7. Definition of the scope of the clinical evaluation (Stage 0) ............................................... 15
8. Identification of pertinent data (Stage 1)........................................................................... 17
8.1. Data generated and held by the manufacturer ................................................................. 17
8.2. Data retrieved 18
9. Appraisal of pertinent data (Stage 2) ................................................................................ 19
9.1. 19
9.2. The appraisal plan ............................................................................................................ 20
9.3. Conduct of 20 政治大纲
9.3.1. How to evaluate methodological quality and scientific validity ......................................... 20
9.3.2. How to determine the relevance of a data t for the 24
9.3.3. How to weight the contribution of each 26
