CRIO is the leader in eSource technology. The system streamlines workflows with a “one system,
one source” approach to clinical data capture. The platform enables electronic data capture and remote monitoring with powerfully integrated solutions that protect data integrity and compliance across 21 CFR 11, ICH-GCP, GDPR, HIPAA, and other global regulations. That’s why over 2,000 sites across the globe have been successful using the CRIO system.
According to a third party survey of CRAs who have used the CRIO system, CRAs favor CRIO over paper by up to 3:1 margins.
With the recent push toward Decentralized Clinical Trials (DCTs), many sponsors are adopting eConsent. eConsent allows patients to consent electronically,
CRIO and strategic partner Jiva Science are providing eSource, Telehealth, eConsent and ePRO in support of a Major Depressive Disorder
Mary Brenner, MSN MArch RN, is CRIO’s Study Design Manager and brings deep-rooted expertise as a registered nurse to CRIO’s
The CRIO Innovation Theater: Creating an EMR to EDC pipeline through eSource, presented insights to a jam-packed audience at DIA’s
BOSTON, MA – August 9, 2022 – CRIO, a Boston-based healthcare technology company streamlining clinical trials for sponsors, sites and
At CRIO, we’re more than “just the tech guys.” In our Q&A series, Ask Me Anything, we caught up with