摘要
目的完善实验室内部复检程序,确保实验室数据准确无误。方法分析药品理化检验复检工作中出现的问题,并对相关部门提出建议。结果与结论药品抽样部门应规范抽样程序,药品标准制订部门应完善质量标准,药品检验机构应提高自身检验能力,确保试验数据准确无误。
Objective To ensure the accuracy of laboratory data,improve the internal retest procedures in the laboratory. Methods Based onquestions of the analysis of physicochemical retest in drug,to provide suggestions to relevant departments. Results and Conclusions Sampling procedures should be standardized in the drug sampling department. Drug standards development departments should improve the quality of standards. Drug testing institutions should improve their ability to ensure the accuracy of the experimental data.
出处
《中国药业》
CAS
2016年第20期19-21,共3页
China Pharmaceuticals
关键词
药品复检
理化检验
不合格药品
retest
physicochemical test
substandard drugs
