摘要
药品检验报告书是药品质量鉴别和仲裁的依据,为了保证药品检验报告书的科学性、准确性、公正性、有效性,必须加强对药品检验报告书的规范化管理。根据长期从事药品检验工作的经验和体会,提出了对药品检验报告书规范化管理的意见。
The medicines survey report is the basis of quality discrimination and arbitrated for medicines. In order to guarantee the science, accuracy, fairness and validity of the medicines survey report, must strengthen the standardized management of the medicines survey report. According to the experience and impressions engaged in work of medicines test for a long time, the author have put forward the suggestion on survey report standardized management of medicines in this article.
出处
《中国药事》
CAS
2007年第7期470-471,共2页
Chinese Pharmaceutical Affairs
关键词
药品
检验报告书
规范化管理
Medicines
Survey report
Standardized management
