摘要
目的探讨GSP现场检查重点问题,为有效提高药品GSP认证质量提供参考。方法对新修订药品GSP实施以来的检查情况进行梳理,讨论现场认证检查过程中应把握的重点环节,分析检查报告中易出现的问题。结果与结论应进一步统一检查标准,检查报告的撰写应更加规范,以更好地对药品经营企业实施监管,建立良好的药品市场秩序。
Objective To discuss the key issues of GSP site inspection, so as to provide a reference for effective improvement of the quality of GSP certification. Methods Based on the elaboration of inspection situation since the implementation of newly revised medicine GSP, the key aspects in GSP-site certification and inspection process that should be grasped were discussed and some common problems in inspection reports were analyzed. Results and Conclusion It is suggested that inspection criteria should be set up and inspection reports be standardized in order to conduct better supervision over pharmaceutical trading enterprises and establish good medicine market orders.
出处
《中国药事》
CAS
2014年第11期1206-1208,共3页
Chinese Pharmaceutical Affairs