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Supporting Monitors & Investigators in Clinical Trials by Incorporating ePRO

March 24, 2015

Recorded Live April 25,2013

In this video, we go over regulatory status and protocol risks facing investigator sites and monitors, new FDA Guidance and GDP implications, how to monitor eCOA data, common issues experienced, materials that reduce compliance issues. Our guest presenter is Jane Carter.

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Successful Management of eCOA Data
Successful Management of eCOA Data

Chapter 2 of a two-part series, providing an overview of electronic data collection. Nora Ibrahimova covers...

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Clinical Outcome Assessments and Your Study
Clinical Outcome Assessments and Your Study

Andrea Murison of Mapi Research Trust joins Paul O’Donohoe to discuss considerations and resources for sele...