Sponsor & CRO
Solutions

Shorten your clinical trial timeline, get instant access to your data, prevent protocol deviations and save on costly monitoring visits! Put your sites on CRIO’s intuitive direct data capture system – the #1 eSource platform among sites worldwide.

Perform real-time monitoring. Build quality into the front end. Lock your data as you go.

Eliminate secondary EDC entry and source data verification

eSource to EDC

eSource to EDC

CRIO’s eSource system sends study data directly to the CRIO Reviewer tool, which CRAs and Data Managers can use to review, query, code, lock and export data. Or, have CRIO funnel the data to your preferred EDC - turning your EDC into an eSource tool.

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EHR/EMR to EDC

EHR/EMR to EDC

Adopt the industry’s first patient-focused, end-to-end EHR-to-EDC data pipeline.

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eConsent

eConsent

CRIO integrates electronic consent directly into the site workflow, automatically “calling” the latest version for initial or re-consent. Manage multiple consent forms and eliminate costly ICF deviations.

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Industry Compliance

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