eConsent
Eliminate outdated forms by auto-tracking consent versions and providing full visibility into patient onboarding.
Time/date-stamped logs, error-proof signatures, and compliance-ready documentation for regulators.
Tracks consent activity while providing a single, easy-to-manage system for study documents.
Participants access digital consent forms via their own devices or at the site.
Patients can read, watch videos, and digitally sign, ensuring a complete understanding.
The system logs time-stamped signatures, tracks ICF versions, and ensures regulatory alignment.
Investigators review and approve consents instantly, eliminating paperwork delays.
Signed consent forms sync automatically with Clinion EDC, ensuring compliance without manual uploads.
AI models tailored for accuracy and precision in clinical research.
Every AI output is logged, traceable, and meets global regulations (ICH, FDA).
Clinion ensures transparency, accountability, and human oversight at every step.
ISO 42001-certified for secure, ethical, and regulatory-aligned AI deployment.