Empower patients and sites with an intuitive eConsent solution that improves education, retention, and adherence, anywhere in the world

Equip your studies with a simple, intuitive informed consent experience designed by clinicians and patient advocates, that can be completed in office with traditional eConsent, or from any remote location with full TeleConsent.

With Medable eConsent, you can:

  • Deploy a tailored consent experience that improves education, retention, and adherence
  • Fast-track your studies in just 12 weeks from kick-off to FPI with Medable’s rapid build and deployment capabilities
  • Fully integrate eConsent with eCOA/ePRO, Televisit and connected devices as well as EDC, EHR, labs and other source data
  • Utilize global support and custom configurations for over 40+ countries, with automatic language detection
  • Author consents and utilize biosample attribution functionality
  • Integrate consent into a larger DCT platform with Televisits, eCOA, and more

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Speak to an eConsent Expert About Your Trials