Using EDC to Answer More than the Primary Endpoint

Clinical trial databases were once used to simply provide the efficacy and safety data for a study. EDC systems are increasingly being expected to support more complex clinical trial designs, adapt to protocol changes and to provide data that is not part of the analysis but assists with, for example, site payments, study monitoring or assists clinical sites with patient management.

In this presentation, Frances Rubenstein will discuss how to effectively implement complex study designs within the M-Core EDC system and how to use the EDC to support other data reporting without collecting an abundance of unnecessary data or interfering with the study's efficacy and safety reporting.
Presented by
Dr. Frances Rubenstein

Director of Database Management, Nevro Corp


Jeffery Doten
Professional Services Project Manager. Medrio

Jeffery Doten is a Professional Services Project Manager at Medrio. Jeffery is an educator, health promotion specialist, and technology enthusiast. He has a Public Health background and has worked in technology since 2008. Over the last 4 years, his focus has been on Clinical Technology software, working with EDC and IWRX platforms to help studies build software, stay on schedule and collect great data. At Medrio, Jeffery’s primary responsibilities center on user education and custom project management.

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