ICH-GCP中英文对照(完整)
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 ...
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...
临床试验中用做对照的试验用药品或市售药物(即阳性对照)或安慰剂。 1.15 Compliance (in relation to trials) 依从性(关于试验的) Adherence to all the trial-related requirements, Good Clinical Practice (GCP) requirements, and the applicable regulatory requirements. ...
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 qual
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 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E6ICHGCP指导原则INTRODUCTION前言GoadClinicalPracticeGCPisaninternationalethicalandscientificqualitystandardfordesigningconductingrecordingandreportingtrialsthatinvolvetheparticipationofhumansubjects.Compliancewiththisstandardprovidespu
ICH-GCP中英文对照(完整).doc,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 par
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