| 2012年中检院化学药品检定所药品评价抽验结果分析 |
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| 引用本文： | 高志峰,朱炯.2012年中检院化学药品检定所药品评价抽验结果分析[J].中国药师,2014(3):470-471. |
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| 作者姓名： | 高志峰 朱炯 |
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| 作者单位： | 中国食品药品检定研究院 北京 100050;中国食品药品检定研究院 北京 100050 |
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| 基金项目： | 中国食品药品检定研究院中青年课题(编号:2012A2) |
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| 摘 要： | 目的：为提高药品评价抽验工作效率与结果运用提出一些建议.方法：对中国食品药品检定研究院化学药品检定所2012年度药品评价抽验总体情况进行汇总,并统计分析.结果：本次抽验中,样品抽取具有代表性,生产企业的不合格率相对较高,同时对不合格项目的成因进行了分析.结论：生产企业应对各环节风险点进行有效控制,监管中应对信息化等环节予以加强.
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| 关 键 词： | 药品 抽验 结果分析 |
| 收稿时间： | 2013/10/23 0:00:00 |
| 修稿时间： | 2013/12/30 0:00:00 |
Result Analysis on Drug Evaluation Inspection of Institute for Chemical Drug Control in 2012 |
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| Gao Zhifeng and Zhu Jiong.Result Analysis on Drug Evaluation Inspection of Institute for Chemical Drug Control in 2012[J].China Pharmacist,2014(3):470-471. |
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| Authors: | Gao Zhifeng and Zhu Jiong |
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| Institution: | (National Institute for Food and Drug Control, Beijing 100050,China) |
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| Abstract: | ABSTRACT Objective: To provide some suggestions for improving the work efficiency and results utilization of Drug evaluation inspection. Methods: The overall situation of the drug evaluation inspection of institute for chemical drug control in 2012 was summarized and statistically analyzed. Results:The sampling was representative, and the unqualified rate in production enterprises was relatively high. The causes of unqualified items were analyzed.Conclusion:Production enterprises should control the process risk points effectively, and the information construction should be strengthened in supervision. |
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| Keywords: | Drug Sampling Result analysis |
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