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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.

Previous Video
Successful Management of eCOA Data
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