# Curebase Curebase eConsent enables interactive consent, e-signatures, and multilingual clinical trial workflows on any device. - Findings24: - Website: - Pricing: Freemium - Categories: Business Software ## What is Curebase? 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. ## What can Curebase do? ### 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. ## Frequently Asked Questions ### 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