浅谈药品生产的变更控制流程

On Change Control Management for Pharmaceutical Production

新版《药品生产质量管理规范》要求制药企业必须建立完善的质量管理体系,在质量管理中变更管理是保证药品质量的重要组成部分,强调在实施GMP时要求企业建立完善的变更控制流程,以保证产品质量。从发起、分析、规划和审批、执行、实施等方面介绍了变更流程。指出制药企业的任何变更都应遵守国家药监局新版GMP变更控制的要求,确保制药标准的权威性,防止随意变换,便于质量追溯及产品质量跟踪,为质量信息系统提供基础信息。

According to the new edition GMP,pharmaceutical enterprises should establish a complete quality management system,in which a change control system is one of the major components. During the GMP implementation process,enterprises are also required to set up a complete control flow for changes to ensure product quality. This paper describes the changing process from the aspects of initiation,plan & approval,execution & following up. It points out that any qualityrelated change in the companies shall conform to the requirements on change control in the new edition GMP issued by the State Food and Drug Administration(SFDA)to maintain the authority of the standard and guard against any freely changing.This will help in the quality tracing and following-up of relative products and provide basic information to the quality information system.