摘要
通过《药品生产质量管理规范》认证,是国家对制药企业必须施行的法规性要求,为在国家规定期限内完成GMP技术改造和软件建设,并顺利通过GMP认证,企业必须有一支精干的技术管理队伍,有对GMP较深刻理解的领导者,有一个清晰的工作思路,有一套行之有效的运行方法,就可以以较短时间、较少投入实现通过GMP认证的目标。
Passing through the certification of <Drug production Quality Management Specification> is a lawful requirement of the state for pharmaceutical enterprises. In order to complete GMP technical transformation and software construction within the period set by the state and pass smoothly through GMP certification. having the small and capable ranks for technical management, the leaders with deep understanding about GMP, the clear working idea, and a set of effective operating methods, the enterprises can realize the target of passing through GMP certification within shorter period of time and with less input.
出处
《科技情报开发与经济》
2003年第10期225-226,共2页
Sci-Tech Information Development & Economy
关键词
GMP认证
中小型制药企业
现代化管理
GMP certification
minor pharmaceutical enterprise
modern management
