Deliver a dynamic and intuitive patient and user experience to support patient trial understanding and compliance and clinician trust.
Improve Patient Enrollment
eConsent drives engagement by educating patients and caretakers about clinical trial information, as well as guiding them through the enrollment process.
Part of the Clinical ink eSource technology, eConsent helps raise patient comprehension, simplify workloads for sites and study teams, and improve data quality to support decision making and regulatory compliance.
Easy-to-follow, patient-friendly eConsent forms deliver tiered information, knowledge checks.
Available with reconsenting triggers, graphical and video content, and translation to 40+ native languages.
Ensure eConsent compliancy using real-time triggers, notifications, progress metrics, and reporting.
Educate and guide patients, minimize errors, and achieve better data quality.
Manage end-to-end eConsent and re-consent processes easily. Monitor patient interactions and ensure they are always kept up to date on protocol changes.
Time and Money
Accelerate your study startup from months to weeks with drag-and-drop authoring tools and rapid prototyping. Minimize strain on your study teams and sites while reducing costs.