eConsent is a secure Electronic Informed Consent solution designed to simplify, standardise, and digitise the patient consent process in late-phase clinical trials. By enabling electronic, multimedia-supported consent—both on-site and remote—eConsent improves patient understanding, accelerates enrolment, and ensures compliant, fully traceable consent management across global studies.
Reduces the risk of missing, duplicate, or outdated documents through centralised management.
Speeds up document review, approval, and retrieval by eliminating manual handoffs and silos.
Maintains continuous inspection readiness with complete, current, and traceable documentation.
Lowers operational and storage costs by replacing paper-based and fragmented document systems.
Applies consistent documentation standards across studies and sites, aligned with regulatory expectations.
Strengthens confidence in regulatory submissions and inspections with audit-ready trial records.
faster consent completion and enrolment timelines
reduction in consent-related errors and rework
improvement in patient understanding and engagement
auditable and compliant electronic consent records
