eConsent

Join the industry’s leader in electronic source data capture for clinical trial sites. CRIO eSource is a user-friendly, web-based tool to capture site source data in real-time.

CRIO Publisher allows sponsors, networks and other users running the same study at multiple sites to build, version and push the templates to the sites on the trial.

CRIO Reviewer allows sponsors and CROs to review eSource data as it's saved, and to query, lock, medical code and extract the data. It's a remote monitoring and EDC tool rolled into one.

CRIO’s eConsent automates the completion and execution of the Informed Consent, and is built right into CRIO’s eSource workflow.

With CRIO’s eRegulatory, research sites can streamline regulatory workflows with paperless binders and an electronic delegation log.

CRIO’s innovative partnership with Pluto Health Health delivers electronic medical records, alongside clinical care insights, straight to the investigator, within minutes! PIs can review health data and insights, and annotate the data before entry into source and the EDC.

CRIO's reporting module lets users filter, sort, search, download, schedule and export data. Users can also have their own Business Intelligence tool query their CRIO data directly.

CRIO’s site-based CTMS lets clinical research sites run their "back office operations", including patient recruiting, scheduling, financial management and more.

Sites can issue and load patient stipend cards with preset or manual amounts. Our reports keep track of how much you’ve paid each subject, enabling easy 1099 reporting.