ICH-GCP中英文对照-完整参考 ICH 三方协调指导原则E6 ICH GCP指导原则INTRODUCTION 前言 Good Clinical Practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects. Compliance with this ...
ICH-GCP中英文对照(完整)
【转自:法迈医讯公众号】
法规|ICH-GCP中英文对照(完整版) 2022 07/08 法迈新媒体 媒体 + 分享 法迈新媒体 A- A+ 指导原则分享 【免责声明】文章为网络整理,不代表“法迈医讯”立场。如因作品内容、版权等存在问题,请于本文刊发30日内联系法迈医讯进行删除或洽谈版权使用事宜。 本文由“健康号”用户上传、授权发布,以上内容(含...
ich-gcp中英文对照(完整)62624 热度: ICH三方协调指导原则E6ICHGCP指导原则 INTRODUCTION 前言 GoodClinicalPractice(GCP)isaninternationalethicalandscientificqualitystandardfordesigning,conducting,recordingandreportingtrialsthatinvolvetheparticipationofhumansubjects.Compliancewiththisstandardprovidespublicassurancethattherights,...
ICH 三方协调指导原则 E6 ICH GCP 指导原则 INTRODUCTION 前言 Good Clinical Practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects. Compliance with this standard provides public ...
ICH 三方协调指导原则 E6 ICH GCP指导原则 INTRODUCTION 前言Good Clinical Practice GCP is an international ethical and scientific quality standard for designing conducting recording and reporting trials that involve the participation of human subject
ICH-GCP中英文对照(完整)ICH 三方协调指导原则E6 ICH GCP指导原则INTRODUCTION 前言 Good Clinical Practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects. Compliance with this standard...
ICH-GCP指导原则的目的是为欧盟、日本和美国提供统一的标准,以促进这些管理当局在其权限内相互接受临床数据。 The guideline was developed with consideration of the current good clinical practices of the European Union, Japan, and the United States, as well as those of Australia, Canada, the Nordic cou...
1、 ICH 三方协调指导原则 E6 ICH GCP指导原则INTRODUCTION 前言Good Clinical Practice (GCP) is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects. Compliance with this standard provides public ...