eConsent

Curebase eConsent is a digital informed consent solution designed for clinical trials. It is intended for both study teams and trial participants, offering a structured consent process that supports compliance requirements while aiming to improve participant understanding and retention.

The platform provides a multimedia-driven consent experience accessible across devices, with tools for study teams to build, manage, and update consent forms without technical complexity. It connects with other components of the Curebase platform, including recruitment, ePRO, scheduling, and notifications.

Participant-Facing Features

• Step-by-step consent flow presented in plain language, accessible on any device
• Support for video, images, and quizzes to help participants understand study information before signing
• Multimedia consent experience designed to be intuitive without requiring prior technical knowledge

Study Team Features

• Drag-and-drop form builder for creating and configuring consent documents
• Version control to manage updates to consent forms over the course of a study
• Re-consent support for situations where participants must review and sign updated consent versions
• Localization tools to adapt forms for different regions and languages
• Support for more than 40 languages with localized formatting

Compliance and Security

• Electronic signature capture with verification and full audit trails
• Meets 21 CFR Part 11 requirements for electronic records and signatures
• Compliant with GDPR standards

Platform Integration

• Consent workflows connect with participant recruitment and engagement tools
• Integrated with ePRO data collection within the same platform
• Links to scheduling and notification features to support the broader trial workflow

Curebase eConsent is part of a broader clinical trial platform that also includes EDC, ePRO, site software, and participant recruitment tools, allowing consent to function as one component within a unified study management environment.