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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
Introduction to Electronic Clinical Outcome Assessments (eCOA)
Introduction to Electronic Clinical Outcome Assessments (eCOA)

<p>Recorded Live January 17, 2013</p>

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

<p>Recorded Live July 25, 2013</p>