The Best Way to Improve Your Clinical Trial Enrollment

eConsent can help you address many difficulties by raising patient comprehension, easing workloads for study teams and sites, and improving data quality to support confident decision-making and regulatory compliance.

The Best Way to Improve Your Clinical Trial Enrollment

eConsent can help you address many difficulties by raising patient comprehension, easing workloads for study teams and sites, and improving data quality to support confident decision-making and regulatory compliance.

The Benefits of eConsent

Easy-to-follow, patient-friendly eConsent forms support tiered information delivery, knowledge checks, reconsenting, graphical and video content, and translation to native languages, among additional features

Realize better data quality, reduce errors, and be certain your eConsent process is compliant with real-time triggers, notifications, progress metrics, and reporting

Manage the end-to-end eConsent and the clinical trial re-consent process by easily monitoring patient interactions and by ensuring patients are always kept up to date on protocol changes

Reduce costs and strain on your study teams and sites and condense your startup time from months to weeks with drag-and-drop authoring tools and rapid prototyping.

Easy Integration with Clinical ink technology simplifies your digital consent and data capture process

Find the real-time status of a clinical trial patient quickly and easily

Dynamic visit creation and conditional logic enhances your eConsent in clinical trials workflow

Required signatures are integrated to ensure clinicians are CFR Part 11 compliant

Additional Clinical Trial Resources

Fact Sheet

eConsent Saves Time and Increases Patient Engagement in Clinical Trial Startup

Read More…

Fact Sheet

eCOA/ePRO Patient Engagement

Read More…

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