摘要
目的:探索研究主数据管理在药品监管领域的应用。方法:介绍主数据及主数据管理相关概念,以药品品种档案为例,提出通过主数据管理思路来建设药品品种档案系统的原理、方法和建议。结果与结论:采用主数据管理思路建设药品品种档案是一种可行方案,通过主数据的分发和共享能够确保不同系统间的数据标准化和一致性,从而促进药品品种档案信息的整合和共享。在我国药品监管信息化建设中,应大力推广主数据管理。
Objective: To discuss the application of master data management in the field of drug regulation. Methods: The concepts of master data and master data management were introduced. The principle, method and suggestions of constructing drug variety file system were put forward through the idea of master data management by taking drug variety files as an example. Results and Conclusion: It was a feasible solution to adopt the concept of master data management to build drug variety files. The distribution and sharing of master data could ensure the standardization and consistency of data among different systems, thus promoting the integration and sharing of drug variety file information. The master data management should be popularized vigorously in the informatization construction of drug supervision in our country.
作者
马进
Ma Jin(Information Center of China Food and Drug Administration,Beijing 100053,China)
出处
《中国药事》
CAS
2018年第9期1172-1175,共4页
Chinese Pharmaceutical Affairs
关键词
主数据管理
药品品种档案
药品监管
信息化建设
master data management
drug variety file
drug regulation
informatization construction