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Global Acceptability

Comply with data, privacy, and regulatory requirements around the world - and utilize our print-to-sign option that preserves the benefits of eConsent even in wet ink signature countries. 

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Fast  & Affordable

The ClinOne platform is easily configured and doesn't require custom development for individual trials. This flexibility allows you to implement eConsent at any scale faster (within 4 weeks), and at a lower cost, than ever before.

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Seamless Integration

Designed to be interoperable with other eClinical systems, ourAPI can easily integrate with other CTMS, eBinders and eRegulatory solutions allowing you to streamline eConsent with your existing workflows.

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Flexible Workflows

Our cloud-based product supports flexible, CFR Part 11 & HIPAA compliant on-site and remote signing workflows and up to 15 unique signer roles and custom signing order to accommodate various site processes.

Key Features You Can Trust

Consent With Virtual Visit

Conduct live virtual visits with up to 10 participants to walk through the consent forms - mirroring an in-person experience.

Real-Time Progress

Access actionable dashboards to see which patients need attention, and track consent progress in real time across the entire trial.

Patient Education

Provide explainer videos,  knowledge checks, and interactive features to facilitate patients comprehension of study requirements.

Document Control

Avoid audit findings & reduce administrative burden by ensuring patients are consented and re-consented on the correct versions.

Request a Quote

Interested in implementing ClinOne's enterprise eConsent solution? Fill out the form to request your custom quote.