Webinar: 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 Medrio 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.

Key takeaways:
  • How EDC functionality is expanding to meet the demands of today’s trials
  • How to effectively implement complex study designs into Medrio EDC
  • How to support crucial supplementary data reporting while keeping safety and efficacy reporting on track

Presented by
Dr. Frances Rubenstein
Director of Database Management, Nevro Corp


Charles Gemora
Senior Solutions Engineer, Medrio

Charles brings years of experience as an expert in eClinical software solutions to our webinar. He has worked closely with data managers and other professionals across the clinical research industry, from pharma to device and beyond, and has gained an insider perspective on the development of ePRO technology. He holds a Bachelor of Science from University of California, Berkeley, and is currently based in Atlanta, GA.

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