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Understanding eConsent and What It Means for Your Clinical Trials


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Webinar Notes

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

Webinar Hosts

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.