摘要
本文就完善药品检验实验室质量体系的组织、职责、文件、管理、考核、重点。
This article made some suggestions on organizations, responsibilities, document construction, management, checking, key-point, countermeasures, and reward or punishment for perfecting the quality system of laboratory for drug control.
出处
《中国药事》
CAS
1999年第1期26-27,共2页
Chinese Pharmaceutical Affairs