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Curebase eConsent is a digital consent tool for clinical trials that delivers interactive consent, captures e-signatures, and supports multilingual workflows on any device.

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Overview

Curebase eConsent is a digital consent tool for clinical trials that turns paper consent packets into an interactive participant experience. It is designed to help study teams deliver informed consent on any device while maintaining the audit trail, version control, and signature handling needed for regulated studies.

The product is part of Curebase’s broader eClinical platform and connects with recruitment, ePRO, EDC, scheduling, notifications, and participant engagement. The source describes it as suitable for studies that need multilingual consent, re-consent workflows, and a structured handoff from consent into the rest of the trial process.

Features

Interactive consent forms

Create step-by-step consent experiences that can include plain language, video, images, and comprehension quizzes to support participant understanding before signing.

Digital signature workflow

Capture electronic signatures with verification, audit trails, version control, and support for 21 CFR Part 11 and GDPR requirements.

Multi-language support

Support consent documents in 40+ languages with localized formatting so studies can serve multilingual populations.

Integrated trial workflow

Connect signed consent to scheduling, notifications, ePRO, recruitment, and other platform workflows without manual handoffs.

Study team authoring tools

Use a drag-and-drop builder with version control and re-consent support to maintain document updates across study lifecycles.

Any-device delivery

Access consent on phone, tablet, or in-clinic iPad, with the same experience available across devices.

Use Cases

  • Participant consent collection

    Replace paper consent packets with a digital experience that can include video, images, and quizzes to help participants understand the study before signing.

  • Consent document updates

    Manage version-controlled consent documents and re-consent workflows when study materials change over time.

  • Global and multilingual enrollment

    Support multilingual studies that need localized consent forms and formatting for participants across different regions.

  • Connected trial workflows

    Move from consent into scheduling, recruitment, and downstream data capture without manual file transfer or re-keying.

  • Any-device consent delivery

    Deliver consent on devices participants already use, or on in-clinic iPads when in-person support is needed.

Pros and Cons

Pros

  • Supports interactive consent experiences with multimedia content and comprehension quizzes.
  • Includes digital signatures, version control, and audit trails for regulated study workflows.
  • Offers 40+ languages and localized formatting for multilingual studies.
  • Works across phone, tablet, and in-clinic iPad use cases.
  • Connects consent to recruitment, ePRO, and scheduling within the same platform.

Cons

  • The source does not provide pricing or plan structure.
  • Integrations are described only within the Curebase platform, with no third-party system list.
  • The evidence focuses on eConsent and related workflows, so broader platform capabilities are only partially documented here.

FAQ

What is Curebase eConsent used for?

Curebase eConsent is built for digital consent workflows in clinical trials. It presents consent content on any device, supports video and images, and includes digital signature capture with audit trails.

How many languages does Curebase eConsent support?

The source states that Curebase eConsent supports 40+ languages and localized formatting.

Is Curebase eConsent compliant with clinical trial regulations?

Yes. The page says Curebase eConsent is designed to meet FDA 21 CFR Part 11 and GDPR standards, with SOC 2 Type II certification also stated on the page.

Can study teams manage and update consent documents in Curebase?

Yes. The page describes a drag-and-drop builder with version control, localization, and re-consent support for study teams.

Does Curebase eConsent connect with other trial workflows?

Yes. The product page says eConsent connects with recruitment, ePRO, EDC, scheduling, notifications, and participant engagement within the same platform.

Quick Facts

Category
eConsent software for clinical trials
Platform
Curebase eClinical platform
Primary users
Study teams, sponsors, CROs, and clinical research sites
Deployment
Web-based, mobile, tablet, and in-clinic iPad access
Compliance
21 CFR Part 11, GDPR, SOC 2 Type II
Source domain
curebase.com