促进我国临床试验数据管理规范化

Translated title of the contribution: Promoting standardization of clinical trial data management in China

吴泰相*, 卞兆祥, 李幼平, 商洪才

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

数据管理制度是影响临床试验质量的主要因素之一,数据管理制度设计包括指导委员会和数据安全与监察委员会、数据采集、数据库、数据安全和监察、数据库锁定五个基本部分。本文介绍各部分的设计要点和方法,旨在帮助广大研究者了解临床试验数据管理制度,吁请广大研究者重视数据管理和了解管理制度的设计,帮助提高临床试验数据的管理水平。

Data management system is a major factor affecting the quality of clinical trial. Development of data management system include a steering group and data safety and monitoring board, data collection, database, performance of the data safety and monitoring, as well as locking of database. This article provides key issues of the five parts so as to help researchers understand the clinical trial data management system.

Translated title of the contributionPromoting standardization of clinical trial data management in China
Original languageChinese (Simplified)
Pages (from-to)532-537
Number of pages6
Journal中国循证医学杂志
Volume18
Issue number6
DOIs
Publication statusPublished - Jun 2018

Scopus Subject Areas

  • Medicine(all)

User-Defined Keywords

  • Clinical trial data
  • Data management
  • Standardization

Fingerprint

Dive into the research topics of 'Promoting standardization of clinical trial data management in China'. Together they form a unique fingerprint.

Cite this