Broader reach, higher engagement, cleaner data.

Total Consent Management

Upgrade to a complete consent management solution for better participant access and experience.

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Expand Global Access to Trials

Accessible on any web-enabled device (BYOD or provisioned), our scalable solution can inform and consent participants anywhere in the world. Flexible enough for any country or site, you can easily collect compliant signatures (digital or wet-ink), on-site or remote with integrated TeleVisit.

Improve Participant Retention

Stay connected with your patients and their data. Real-time notifications help ensure compliance while patient and caregiver-friendly ePROs make it easy for sponsors to track toxicity and tolerability in real time.

Minimize Compliance Errors

Gain complete visibility and oversight into your trial with real-time monitoring of all consent activities within a single dashboard and ensure inspection-ready audit trails with fully integrated template management and version control.

Medable participant on laptop device

Introducing Total Consent

  • Self-service authoring tool to easily create engaging consent templates
  • Biosample attribution to confirm storage permissions for consent objects
  • Permission-based workflows by roles and responsibilities for secure control
  • Designed to comply with all global regulations, including FDA 21 CFR Part 11, ICH E6 (R2), and GDPR