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浅谈药品监管主数据体系架构设计 被引量:1

Preliminary Analysis of Master Data Framework Design for Drug Supervision
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摘要 目的:探索设计药品监管主数据体系架构。方法:介绍主数据概念、优势及实施情况,从组织体系、考核体系、标准体系、集成体系、安全体系等五方面设计药品监管主数据体系架构。结果与结论:主数据是一个部门的核心数据资源,对于加强数据统一管理、交互共享、协同应用以及统计分析等具有非常重要的作用,主数据管理要做的并不只是建设一个信息系统,而是要建立一套适用于药品监管领域的主数据体系架构。 Objective: To Explore the designs of the master data framework for drug supervision. Methods: The concept, advan- tages and implementation of the master data were introduced. The designs of the master data framework for drug supervision were performed from five aspects including organization system, assessment system, standard system, integration system and security system. Results and Condusion: The master data is the core data resource of a department. It plays a very important role in strengthening the unified management of data, sharing interaction, cooperative application and statistical analysis. The master data management is not only to build an information system, but also to establish a set of master data framework suitable for the field of drug supervision.
作者 马进 陈罡毅 Ma Jin;Chen Gangyi(Information Center of China Food and Drug Administration,Beijing 100053,China;University of Inter-national Business and Economies)
出处 《中国药师》 CAS 2018年第11期2017-2019,共3页 China Pharmacist
关键词 主数据 主数据管理 标准 安全 Master data Master data management Standard Security
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