eConsent
A Smarter Way to Manage Patient Consent –
Building Patient Trust and Compliance from the Start.
Eliminate Consent Errors & Delays - Digitize with Clinion eConsent
Traditional consent is slow, error-prone, and burdensome, impacting patient enrollment. Clinion eConsent enhances engagement and compliance with digital access, real-time tracking, and seamless EDC integration for a patient-centric, audit-ready process.
With enhanced flexibility for sponsors, control for sites, and a seamless experience for patients, Clinion eConsent ensures trials start strong and stay compliant.
Reduce setup timelines from months to weeks and automate re-consenting for protocol amendments, avoiding delays or regulatory audit findings.
Auto-track consent versions, monitor patient onboarding in real-time, and maintain audit-ready logs with time-stamped signatures and compliance-proof documentation.
Enhance patient enrollment and engagement with a transparent, user-friendly consent process that improves understanding, boosts retention and ensures compliance.
Patient Reviews Consent
Participants access digital consent forms via their own devices or at the site.
Interactive & Informed Decision-Making
Patients can read, watch videos, and digitally sign, ensuring a complete understanding.
Automated Compliance Tracking
Time-stamped signatures, ICF version control, and regulatory compliance tracking are managed effortlessly.
Seamless Site Oversight & Approval
Investigators review and approve consents instantly, eliminating paperwork delays.
Built for Every Stakeholder - One eConsent, Multiple Benefits
Intuitive & Engaging Patient Experience
A user-friendly UX with embedded questions and live support ensures clear understanding. The system automates the delivery of digitally signed eConsent for secure record-keeping.
Tailored for Site
Efficiency
Reduce administrative burden with configurable eConsent, offering standardized ICFs and site-specific customization to align with trial requirements and streamline processes.
Full Flexibility & Control for Sponsors
Ensure compliance and adaptability with remote editing, automated patient re-consenting, and transparent version control, all backed by audit-ready documentation.
Multilingual & Multi-Platform Accessibility
With multilingual support and seamless compatibility across iOS, Android, and tablet platforms, it ensures a smooth and consistent user experience worldwide, enhancing accessibility.
Revolutionize Patient Consent –
Easy, Fast & Built for Modern Clinical Trials
patient-friendly experience – making consent smarter, faster, and fully regulatory-ready.