摘要
本文通过对近期药品委托生产的检查情况及变更情况进行汇总,结合企业调研情况及国外委托生产和变更控制的监管机制分析,探讨我国药品委托生产中变更管理的策略,以此提高药品委托生产现场检查的检查效率,为保证检查质量和药品质量安全提供技术支持,也为药品生产企业提供有效的技术指导。药品委托生产是产业发展的必然趋势,但当前的委托生产仍然存在一些问题,发生变更是一个常见现象,监管部门应从技术监管方面加以严格管理,不断完善相关法规政策,解决实施过程中出现的问题,以便更好的规范药品委托生产,确保药品质量安全。
Strategies for change management in contract manufacturing of drugs in China were discussed based on the recent inspection of contract production of drugs and the change summary analysis combined with the supervision mechanism of domestic and foreign enterprises in contract production of drugs so as to improve the inspection efficiency of the commissioned production site inspection and provide technical support for ensuring the quality of inspection and drug quality and safety and also effective technical guidance for the pharmaceutical production enterprises. Contract production of drugs is the inevitable trend of industrial development, however, there still exist some problems in it. So the change is a common phenomenon, strict management should be implemented from technical supervision by government regulators, and the relevant regulations and policies should be constantly improved to solve the problems happened in the implementation process so as to better regulate the contract production of drugs and to ensure drug quality and safety.
出处
《上海医药》
CAS
2017年第17期42-45,共4页
Shanghai Medical & Pharmaceutical Journal
关键词
药品委托生产
变更
评价分析
策略
contract manufacturing of drugs
change
evaluation and analysis
strategy