FACT SHEET
Deliver a dynamic and intuitive patient and user experience to support patient trial understanding and compliance and clinician trust.
eConsent
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.
eConsent Benefits
Optimize
Patient Experience
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.
Improve
Consent Process
Ensure eConsent compliancy using real-time triggers, notifications, progress metrics, and reporting.
Educate and guide patients, minimize errors, and achieve better data quality.
Reduce
Site Workload
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.
Save
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.
Eliminate
Separate Systems
Integrate across Clinical ink eSource technology – DDC, ePRO, eCOA – to simplify end-to-end data capture processes.
Evaluate
Patient Snapshots
Access and monitor real-time status of a clinical trial patient quickly and easily.
Improve
Workflows
Enhance eConsent with dynamic visit creation and conditional logic across clinical trials workflows.
Ensure
Compliance
Ensure clinicians are CFR Part 11 compliant with signature requirements integration.
