Integrated eClinical workflows
Connect recruitment, eConsent, eCOA/ePRO, participant engagement, and EDC in one clinical trial platform.
Curebase
Curebase réunit recrutement, consentement électronique, eCOA/ePRO, engagement des participants, EDC et IA dans une plateforme eClinical.
Qu'est-ce que Curebase ?
Curebase is an eClinical platform for biotech, medtech, pharmaceutical companies, CROs, and research sites. It connects participant recruitment, eConsent, eCOA/ePRO, engagement, and electronic data capture (EDC), rather than being only a consent tool.
Its integrated AI voice agent Hope supports multilingual outreach, appointment scheduling, reminders, and escalation to study coordinators. EDC supports forms, queries, adverse-event records, data review, and study data exports. eConsent is one module: it provides interactive consent, electronic signatures, document versioning, re-consent, and more than 40 languages. Study teams should confirm the modules, validation requirements, and deployment scope needed for their trial.
Que peut faire Curebase ?
AI participant engagement
Hope supports multilingual voice outreach, scheduling, reminders, and routing follow-up to study coordinators.
Electronic data capture
EDC supports study forms, adverse-event records, data queries, review, and exports.
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.
Cas d'utilisation
“Integrated eClinical workflows”
Connect recruitment, eConsent, eCOA/ePRO, participant engagement, and EDC in one clinical trial platform.
“AI participant engagement”
Hope supports multilingual voice outreach, scheduling, reminders, and routing follow-up to study coordinators.
“Electronic data capture”
EDC supports study forms, adverse-event records, data queries, review, and exports.
“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.
Questions fréquentes
What is Curebase?
Curebase connects recruitment, eConsent, eCOA/ePRO, participant engagement, EDC, and AI tools in one eClinical platform.
Which workflows can a study team connect?
Recruitment, electronic consent, participant-reported outcomes, engagement, and EDC can be combined according to the study scope.
How is Curebase priced?
Prices are not publicly listed. Contact Curebase to discuss study requirements, modules, and a quote.
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.
Informations rapides
- Category
- eClinical platform
- 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
Analyse du trafic de Curebase
Les données de trafic sont fournies à titre indicatif uniquement.
- Évaluation du domaine
- 47
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