摘要
本文介绍了我市对质量管理工作的药品入库验收、药品在库养护、药品出库复核,销售后的质量跟踪等12个方面的文书档案的具体规定,以推动质量管理工作的标准化、规范化。
This article introduces the specific stipulations for 12 categorories of quality control archives, such as acceptance for drug storage, storing drugs under appropriate conditions, checking up on drugs released from the storehouse, and post-marking quality surveillance, in order to promote the standardization and normalization Of quality control.
出处
《中国药事》
CAS
1993年第4期203-206,共4页
Chinese Pharmaceutical Affairs