目前药品生产企业在药品生产质量管理规范的实施过程中，生产场地消毒管理方面存在的问题比较突出。消毒相关缺陷出现频率较高的问题包括消毒策略制定、消毒验证、消毒程序文件、消毒执行、消毒剂管理。对药品生产企业药品生产现场的消毒相关缺陷进行分析，并提出改进建议，以期为药品生产企业提升消毒管理提供借鉴。

At present, there are prominent problems in disinfection management of drug production sites in the implementation of GMP by pharmaceutical manufacturers. Disinfection related deficiencies occur frequently, including disinfection strategies formulation, disinfection validation, disinfection procedure documents, disinfection execution, and disinfectant management. This article analyzes the disinfection related deficiencies in drug production sites of pharmaceutical manufacturers and proposes improvement suggestions, in order to provide reference for pharmaceutical manufacturers to improve disinfection management.

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