| 简述我国进口药品注册检验工作的历史、现状及展望 |
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| 引用本文： | 王岩,马双成,王雅雯.简述我国进口药品注册检验工作的历史、现状及展望[J].中国药事,2009,23(8):770-773. |
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| 作者姓名： | 王岩 马双成 王雅雯 |
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| 作者单位： | 中国药品生物制品检定所,北京,100050 |
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| 摘 要： | 目的介绍我国进口药品注册检验工作。方法从法律法规、工作内容、指导原则等多方面简要介绍进口药品注册检验管理的方法与经验。结果与结论通过对现阶段管理方式的分析，为进一步改进我国进口注册检验工作提供建议。
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| 关 键 词： | 进口药品 注册检验 现状 |
Brief Introduction of Validation and Verification of Quality Specification of Import Drug in China |
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| Wang Yan,Ma Shuangcheng,Wang Yawen.Brief Introduction of Validation and Verification of Quality Specification of Import Drug in China[J].Chinese Pharmaceutical Affairs,2009,23(8):770-773. |
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| Authors: | Wang Yan Ma Shuangcheng Wang Yawen |
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| Institution: | (National Institute for the Control of Pharmaceutical and Biological Products, Beijing 100050) |
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| Abstract: | Objective Brief introduce the validation ＆ verification of quality specification of import drug in China. Methods Participate the experience through the legislations, content, guideline etc. Results and Conclusions To analyze successful experience, proposed work in future |
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| Keywords: | import drug validation verification of quality specification current situation |
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