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随着网络技术和自动化技术的普及和发展,越来越多的商家和企业开始通过电子记录实现对产品质量和产品生产的管理。为加强企业对电子记录系统的运用,本文研究了药品生产质量管理(GMP)和电子记录的使用准则及相关内容,提出了现阶段制药生产企业电子记录在药品生产质量管理方面存在的问题,并在此基础上提出了相关建议及对策。
With the popularization and development of network technology and automation technology, more and more businesses and enterprises begin to manage product quality and product production through electronic records. In order to strengthen the use of electronic record system by enterprises, this paper studies the usage rules and related contents of GMP and electronic records, and puts forward some problems in the current pharmaceutical manufacturing enterprises electronic record in the quality control of drug production. On this basis, put forward relevant suggestions and countermeasures.