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    Next-Gen eConsent Software

    Modern, User-Friendly eConsent for Clinical Trials

    Deliver fully informed consent with a digital experience that's intuitive for participants, easy to set up for study teams, and built to support compliance and retention from the start.

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    21 CFR Part 11 Compliant
    GDPR Compliant
    SOC 2 Compliant
    eConsent signature interface showing patient and investigator workflow

    Streamlined eConsent for Understanding and Compliance

    Simple for Participants

    Streamlined, multimedia consent experience across any device

    Digital Signature Capture

    Secure, compliant electronic signatures with verification and audit trails

    Multi-language by Design

    Support for 40+ languages and localized formatting

    Interactive Consent Forms

    Video, images, and quizzes to help participants understand before signing

    Integrated Experience

    Seamlessly connects with scheduling, notifications, ePRO, and more

    Built for Compliance

    Meets 21 CFR Part 11 and GDPR standards with full audit trails

    eConsent Is the Front Door to Every Trial

    The consent moment shapes everything that follows: how well participants understand the study, how confident they feel signing on, and how quickly they make it to their first visit. Curebase eConsent replaces dense paper packets with an interactive, plain-language experience that meets each participant where they are.

    Because eConsent is built into the same platform as ePRO, EDC, and participant engagement, every signed consent flows directly into the workflows that follow, no manual hand-offs and no orphaned PDFs.

    40+ languages
    localized consent forms out of the box
    21 CFR Part 11
    validated electronic signatures and audit trails
    Any Device
    phone, tablet, or in-clinic iPad supported

    How It Works

    1

    For Participants

    Step-by-step consent with video, images, and plain language, on any device

    2

    For Study Teams

    Drag-and-drop builder with version control, localization, and re-consent support

    3

    Fully Integrated

    Consent connects with recruitment, engagement, and ePRO in one structured platform

    Built for Compliance

    Curebase eConsent is designed to FDA 21 CFR Part 11 and ICH GCP standards, with validated electronic signatures, version-controlled consent documents, role-based access, and a complete audit trail of every view, edit, and signature event.

    The platform is GDPR-compliant and SOC 2 Type II certified, supporting global multi-site studies across regulatory jurisdictions.

    Where eConsent Fits

    eConsent is one piece of Curebase's structured eClinical platform. It connects directly with recruitment, ePRO, EDC, and participant engagement, so signed participants flow into screening, first-visit scheduling, and ongoing data collection without manual data transfer or re-keyed records.

    Why Digital eConsent Outperforms Paper Consent

    Paper ConsentCurebase eConsent
    ComprehensionDense text onlyVideo, images, and comprehension quizzes
    Re-consentManual reprint and re-collectionAutomated workflow with tracked acknowledgment
    Signature integrityWet-ink scans with manual filingValidated digital signatures with identity verification
    LanguagesPer-site translation logistics40+ languages built in
    Audit trailManual binders and version drift21 CFR Part 11 audit trail end to end

    Frequently Asked Questions

    Ready to See It in Action?

    See how Curebase can transform your clinical trials.

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