Streamline your site's operations.
Access clinical trial data anywhere.

Imagine this: your clinical trials fully free from paper binders, so you can access source data remotely, collaborate in real-time, add virtual “sticky notes,” track your finances, and manage your patient recruiting. This, all in a sleek interface that you and your colleagues will find robust yet intuitive.

With CRIO’s clinical trial software, it’s possible — learn how below.

Comprehensive, Compliant Clinical Trial Software, Built For Your Site

  • CTMS
  • eSource
  • eRegulatory
  • eConsent

CTMS

Boost your clinical trial management with our intuitive software. Configure budgets to automate receivables, holdbacks and screen failure caps. Use one-click calls & text to recruit patients, schedule visits, and more.

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eSource

CRIO’s flagship electronic source is popular among thousands of research sites. Capture source data with a tablet or computer, ensure data accuracy, collaborate in real time, and enable remote monitoring.

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eRegulatory

Streamline your clinical trial regulatory workflows with paperless binders and the first-ever Electronic Delegation Log. Store, route, and bulk eSign documents, manage certifications and trainings, and more.

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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

Learn More About CRIO

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