您好,欢迎您来 医疗器械临床试验 医疗器械 注册 临床试验 FDA510k CE 咨询 龙德!   请登录| 立即注册| 会员中心| 收藏本公司 | 设为主页

欧盟CE法规

【Guidance】MEDDEV 2.7 / 2-临床调查,临床评估 - 主管当局对临床调查通知进行评估的指南

2017/11/23


MEDDEV 2.7/2 rev.2  Guidelines for Competent Authorities for making a validationassessment of a clinical investigation application under directives 90/385/EEC and 93/42/EC
指导性文件医疗器械 - 临床调查,临床评估 - 主管当局对临床调查通知进行评估的指南 - MEDDEV 2.7 / 2

2015年9月发布


标题点击download
下载附件

Guidance document Medical Devices - Clinical investigation, clinical evaluation - Guide for Competent Authorities in making an assessment of clinical investigation notification - MEDDEV 2.7/2Download PDF rendition (413.889)


原文链接:MEDDEV 2.7/2 rev.2  Guidelines for Competent Authorities for making a validationassessment of a clinical investigation application under directives 90/385/EEC and 93/42/EC(点击进入)

换一张