摘要
目的:研究美国食品药品监督管理局(FDA)药品监管法规文件数据库的构建,为完善我国药品监管法规文件数据库提供参考。方法:详细介绍FDA药品监管法规文件数据库的构成及功能,为我国数据库的进一步完善提出建议。结果与结论:FDA网站建立了相对完善的药品监管法规文件数据库,其结构的逻辑性、资源的完整性及检索功能的便捷性均存在可借鉴之处。我国正在探索建设、完善药品法规数据库,其系统性与科学性需要不断提高,从而更好地满足公众及行业需求。
Objective:To study the construction of regulation document database of FDA in order to provide references for the improvement of drug regulation document database in China.Methods:The constitution and functions of the database of drug regulation documents of FDA were introduced in detail,and some suggestions for the further improvement of database in China were put forward.Results and Conclusion:FDA website has established a relatively complete database of drug regulation documents,which can be used for reference in the logicality of structure,integrity of resources and convinience of retrieval functions.China is trying to build and perfect the database of drug laws and regulations,but the systematicness and scientificity need to be improved so as to better meet the needs of the public and the industry.
作者
张静
关月月
揣红梅
唐桃群
潘威
杨悦
Zhang Jing;Guan Yueyue;Chuai Hongmei;Tang Taoqun;Pan Wei;Yang Yue(Center for Information,NMPA,Beijing 100044,China;School of Business Administration,Shenyang Pharmaceutical University,Shenyang 110016,China;School of Pharmacy,Tsinghua University,Beijing 115003,China)
出处
《中国药事》
CAS
2021年第12期1414-1418,共5页
Chinese Pharmaceutical Affairs
基金
国家药品监督管理局信息中心委托课题(编号CFDAIC-XXFW-201896)。