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药品检验报告书缺陷及规范化书写

同晓霞 任慧

中国药业2016,Vol.25Issue(18):14-15,16,3.
中国药业2016,Vol.25Issue(18):14-15,16,3.

药品检验报告书缺陷及规范化书写

Discussion on the Defects and Standardized Writing of Drug Inspection Report

同晓霞 1任慧1

作者信息

  • 1. 陕西省延安市药品检验所,陕西 延安 716000
  • 折叠

摘要

Abstract

Objective To improve the overall level of drug inspection. Methods Common defects and standardized writing in the drug inspection report were introduced,the need for standardization were analyzed,and therecommendations for standardized writing were pro-vided. Results The current reports had various and non-standard forms in different provinces,and further supplement and perfection were needed. Conclusion Drug inspection personnel should be seriously complete the drug inspection report and avoid casually writ-ing;the results of each test must be carefully checked to avoid errors and defects.

关键词

药品/检验报告书/缺陷/规范化

Key words

drug/drug inspection report/defect/standardization

分类

医药卫生

引用本文复制引用

同晓霞,任慧..药品检验报告书缺陷及规范化书写[J].中国药业,2016,25(18):14-15,16,3.

中国药业

OACSTPCD

1006-4931

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