Product Overview
Review, query and lock visits in real-time
Clinical monitors can perform full source data review, issue/close queries, and mark visits as reviewed. CRIO’s system solicits PI signatures contemporaneously, allowing the sponsor team to continuously lock visits, enabling faster data locks.
Perform medical coding
CRIO has built-in WHODrug and MEDDRA dictionaries, with coding and review workflows. Sponsors can even embed the medication list at point of capture to increase autocoding and accelerate the coding workflow!
Review uploaded site PDF files
Reviewer also lets the clinical team review uploaded PDFs, including executed CRIO eConsent forms and EMR records, plus any other files uploaded by research sites. Review, query and lock the files, just as with direct data capture.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
Unlike paper source, CRIO’s eSource is interactive, guiding the sites along the appropriate workflow path. With built in edit checks and branching logic, the template ensures that sites are adhering to the protocol and collecting data accurately and completely. An automated audit log ensures full attribution. Thus, CRIO’s eSource builds quality into the front-end data collection process – unlike the eCRF, where the edit checks only trigger after the secondary data is entered, which is many days, weeks if not months, after the patient visit is complete. And when the site disregards the system’s built-in alerts, CRIO converts the alert into an auto-query.
About the company
Founded in 2015 by current CEO Raymond Nomizu and Phuc Truong, CRIO’s goal is to transform the clinical trial industry by reimagining workflows from a site-centric perspective. By automating protocols at the site level, CRIO’s technology builds quality at point of capture, unlocking significant downstream benefits for sites and sponsors alike.
