文章摘要
郭俊荣,梁欣,李江帆,庞宏贤,贺晓辉,王旭红,邵鑫迪.首都医科大学附属北京潞河医院I期临床试验药房试验用药品管理模式分析与探讨[J].中国药事,2023,(8):966-969
首都医科大学附属北京潞河医院I期临床试验药房试验用药品管理模式分析与探讨
Analysis and Discussion on the Management Mode of Experimental Drugs in the Phase I Clinical Trial Pharmacy of Beijing Luhe Hospital Affiliated to Capital Medical University
投稿时间:2022-07-07  
DOI:10.16153/j.1002-7777.2023.08.015
中文关键词: 试验用药品管理  临床试验  质量管理  冷链系统  信息管理
英文关键词: experimental drug management  clinical trial  quality control  cold chain system  information management
基金项目:2022年北京市通州区科委课题 “利用智能化技术建立药物临床试验合并用药医嘱预警系统” (编号 KJ2021CX008-01)
作者单位
郭俊荣 首都医科大学附属北京潞河医院北京 101149 
梁欣 首都医科大学附属北京潞河医院北京 101149 
李江帆 首都医科大学附属北京潞河医院北京 101149 
庞宏贤 首都医科大学附属北京潞河医院北京 101149 
贺晓辉 首都医科大学附属北京潞河医院北京 101149 
王旭红 首都医科大学附属北京潞河医院北京 101149 
邵鑫迪 天津医科大学天津 300070 
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中文摘要:
      目的:探讨首都医科大学附属北京潞河医院Ⅰ期临床试验药房试验用药品管理模式,总结经验和分析不足,为其他临床试验机构中心药房管理模式提供参考。方法:本文分析总结了Ⅰ期临床试验药房基本情况、试验用药品管理流程、智能冷链监控系统的使用、药物信息化管理等。结果与结论:首都医科大学附属北京潞河医院Ⅰ期临床试验药房不同存储区域可满足试验用药品不同温度存储要求。采用智能冷链温度监控系统监测24 h环境及仪器设备温度,可及时发现超温情况,能尽早采取措施,将试验风险降到最低。试验用药品的电子化管理可在线动态管理与实时记录,提高数据管理的安全性和可靠性, 方便数据溯源,提高数据质量。
英文摘要:
      Objective: To explore the management mode of experimental drugs in the Phase I clinical trial pharmacy of Beijing Luhe Hospital affi liated to Capital Medical University, summarize the experience and analyze the insufficiency, and provide references for the management mode of the central pharmacy of other clinical trial institutions. Methods: The basic situation of Phase I clinical trial pharmacy, the management process of experimental drugs, the use of intelligent cold chain monitoring system, and drug information management were analyzed and summarized in this article. Results and Conclusion: The diff erent storage areas of Phase I clinical trial pharmacy in our hospital can meet the storage requirements of experimental drugs at diff erent temperatures. The intelligent cold chain temperature monitoring system is used to monitor the temperature of the environment and equipment for 24 hours, so that the over-temperature situation can be detected in time, and measures can be taken as early as possible to minimize the risk of the test. The electronic management of experimental drugs can be dynamically managed online and recorded in real time, which improves the safety and reliability of data management, facilitates data traceability, and improves data quality.
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