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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

<p>Recorded Live February 21, 2013</p>

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

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

CRF Health and University Hospital Basel Collaborate to Create Electronic Version of the Neurostatus-EDSS

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