Webinar: Understanding eConsent and What It Means for Your Clinical Trials

Better patient engagement through eConsent

Clinical research is on the cusp of an eConsent revolution. With benefits ranging from lower costs and better patient engagement, and with major regulatory bodies pushing for improvements to the informed consent process, there has never been a better time to start developing your eConsent strategy. Join our webinar to learn how you can leverage eConsent to enhance your trials.

Key takeaways:
  • Learn how improving the consent process leads to lower costs and better patient retention
  • Get best practices for eConsent selection and see a live demonstration of a real platform
  • Understand how regulatory shifts are driving interest in eConsent around the world
Presented by
Gabriel Westerlund
Solutions Engineer, Medrio

Gabriel Westerlund is a data-driven and creative problem solver with a passion for technology. As a Solutions Engineer at Medrio, he is the go-to technical expert for product demonstrations, customer implementations, trainings, and more. Gabe holds a Bachelor of Science from Uppsala Universitet in Uppsala, Sweden, and is based out of Medrio's San Francisco headquarters.

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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