Multimedia for real understanding
Video, visuals, and voice guidance replace dense legal text, so participants know what they’re consenting to.
eConsent
Clear, multimedia-guided consent patients can actually understand. Built for global enrollment, hybrid trials, and real-time oversight, without adding burden to sites.
Most eConsent platforms digitize PDFs. Delve rethinks consent with multimedia, comprehension checks, human support, and real-time site oversight, so every participant truly understands the study.
Video, visuals, and voice guidance replace dense legal text, so participants know what they’re consenting to.
Full audit trails, version control, and signature verification, aligned with FDA, EMA, and ICH E6(R3) guidance.
Concierge teams help patients during consent, answering questions, resolving issues, and ensuring complete documentation.
Video, audio, images, simplified text, and chapter-style navigation. Designed for every literacy level and culture, not just English-speaking populations.
Built-in comprehension checks confirm understanding, and every step is documented for inspection.
When a patient pauses, drops off, or fails a comprehension quiz, a Delve coordinator reaches out. Fewer delays, higher completion.
See who started consent, who finished, and who needs help, while there’s still time to act.
Live visibility into who started consent, who completed it, and who needs follow-up.
Automatic notifications when patients pause or fail to complete a section.
Sites, monitors, and sponsors see only what they need, nothing more.
HIPAA, GDPR, and 21 CFR Part 11-aligned consent storage with audit history. 100% regulatory audit-ready.
How a Delve consent flow runs, and what keeps it inspection-ready.
The patient watches a short consent video and reviews key sections with visuals.
Comprehension checks confirm understanding and reduce re-consent risk.
eSignature is captured with versioning and an audit-ready record.
Sites and sponsors follow progress in real time and step in when a patient pauses.
Effective eConsent is more than a signature. It has to protect comprehension, regulatory integrity, and a complete record of what the participant saw and signed.
Aligned with FDA, EMA, and ICH E6(R3) guidance for electronic informed consent.
Version control, time-stamped records, IP logs, and signature certificates.
HIPAA, GDPR, and 21 CFR Part 11-aligned storage with role-based access.
Operational guides on consent, enrollment, and patient support.
A practical guide to running consent and outcome assessments on one platform.
Read →Where site workload comes from in decentralized and hybrid designs, and how to take it off.
Read →How language coverage and cultural fit protect data quality in global trials.
Read →Multimedia, human support, and real-time oversight. Everything you need to start patients on the right path.
Book an eConsent demo