数据完整性的“指南针”——MHRA发布GMP数据完整性指南精读.docx

?欧洲药典在线27.1征求意见（截20150114?3各论将自2016年1月1日起撤出EP201501 MHRA数据完整性指南2015-01-29 21:33:23|??分类：EDQM|??标签：|举报|字号大中小?订阅MHRA GMP Data Integrity Definitions and Guidance for Industry January 2015MHRA的GMP数据完整性定义和行业指南/2015年1月Introduction: 背景介绍Data integrity is fundamental in a pharmaceutical quality system which ensures that medicines are of the required quality. This document provides MHRA guidance on GMP data integrity expectations for the pharmaceutical industry. This guidance is intended to complement existing EU GMP, and should be read in conjunction with national medicines legislation and the GMP standards published in Eudralex volume 4. 数据完整性在药品质量体系中是基本要求，它保证药品具有所需要的质量。本文件向制药行业提供MHRA关于GMP数据完整性方面期望的指南。本指南意在对现有EU GMP进行补充，应与国家药监法规和欧洲法规第4卷的GMP标准联合解读。The data governance system should be integral to the pharmaceutical quality system described in EU GMP chapter 1. The effort and resource assigned to data governance should be commensurate with the risk to product quality, and should also be balanced with other quality assurance resource demands. As such, manufacturers and analytical laboratories are not expected to implement a forensic approach to data checking, but instead design and operate a system which provides an acceptable state of control based on the data integrity risk, and which is fully documented with supporting rationale. 数据管理系统应与EU GMP第1章中描述的药品质量体系相结合。给数据管理提供的努力和资源应与产品质量的风险相称，还应与其它质量保证资源需求相平衡。因此，并不期待生产商和分析实验室实施一种辩论的方法来对数据进行检查，而只需要设计和实施一种系统，提供一种基于数据完整性风险的可接受控制状态，并对支持性理由进行完整记录。Data integrity requirements apply equally to manual (paper) and electronic data. Manufacturers and analytical laboratories should be aware that reverting from automated / computerised to manual / paper-based systems will not in itself remove the need for data integrity controls. This may also constitute a failure to comply with Article 23 of Directive 2001/83/EC, which requires an authorisation holder to take account of scientific and technical progress and enable the medicinal produc