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作 者:张丽丽 赵婧 郭建怡 石坚 江志杰 Zhang Lili;Zhao Jing;Guo Jianyi;Shi Jian;Jiang Zhijie(Beijing Institute for Drug Control,NMPA Key Laboratory for Research and Evaluation of Generic Drugs,Beijing Key Laboratory of Analysis and Evaluation on Chinese Medicine,Beijing 102206,China)
机构地区:[1]北京市药品检验研究院,国家药品监督管理局仿制药研究与评价重点实验室,中药成分分析与生物评价北京市重点实验室,北京102206
出 处:《首都食品与医药》2024年第4期113-115,共3页Capital Food Medicine
摘 要:目的 探讨药品检验机构留样库房管理的合理性,以满足受理药品的贮藏要求,保证检验结果准确可靠,推动药品检验机构持续发展.方法 分析国内外药品贮藏要求的差异,梳理药品检验机构库房管理现状,探析留样库房管理要点.结果 和结论 药品检验机构库房设置合理,关键环节的管理经验丰富,应持续探讨未来管理发展趋势.Objective Exploring the rationality of sample storage management in drug inspection institutions to meet the storage requirements of accepted drugs,ensure the accuracy and reliability of inspection results,and promote the sustainable development of drug inspection institutions.Methods Analyze the dfferences in drug storage requirements at home and abroad,sort out the current situation of warehouse management in drug inspection institutions,and explore the key points of sample storage management.Results and Conclusion The warehouse settings of drug inspection institutions are reasonable,and the management experience in key links is rich.Future management development trends should be continuously explored.
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