Drug Adverse Events Surveillance with CDISC Standards for Multiple Trials

Time

Mon, Jun 25 11:00AM
M 14

Title

Drug Adverse Events Surveillance with CDISC Standards for Multiple Trials

Abstract Summary

By using our web-based EDC system adopted CDISC standards, we consolidated 17 clinical trial databases conducted from 2008 to 2010. Then, adverse events data structure and contents are analyzed to investigate current status of standard data in terms of drug safety evaluation.

Poster Presenter

Boram Wang
MPH,
The Catholic University of Korea
Korea, Republic of

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