“I absolutely love CRIO. I cannot picture running a multi-specialty research site without it.”
“We have been able to grow our operations with one less person than we would normally have had. Between the employee savings and the paper cost savings, we literally come out ahead on a P&L
basis. CRIO is not a cost item but a savings generator.”
“With CRIO, I save so much time that sometimes at 3pm, I’m looking for things to do. Now, I have capacity to take on more studies, and I don’t have to turn away something that could otherwise be financially rewarding.”
“Our monitors have really embraced this because they can perform remote monitoring much more easily, and when they leave a comment, it’s electronic so they can always see it. We used to get into disputes sometimes because they would say they left a sticky, but we didn’t see it.”
“These were long-time veterans who have seen a lot of things, so they have a healthy degree of skepticism. So when they came back gushing about the system, I knew I had to take it seriously.”
Capture source data seamlessly and in real-time with CRIO’s best-in-class electronic source. You’ll eliminate up to 90% of your paper and improve data quality by 80%.
Learn MoreTake control of your operations with CRIO’s intuitive Clinical Trial Management System. Schedule patients, track financials, streamline recruiting, and more.
Learn More
Introducing electronic regulatory binders fit for the 21st century, which includes the first-ever electronic delegation log — all 21 CFR Part 11 compliant.
Learn MoreFor clinical trial sponsors: conduct 100% remote monitoring of your sites’ source data and regulatory documents in a secure, online portal.
Learn MoreBecause of built-in edit checks, branching logic and other automations, CRIO’s system cuts down on errors and omissions at the point of data capture. Thus, QC review and EDC entry become smoother and faster.
We don’t have to do any more sticky notes.... it saves us a lot of misery, and the staff picked up on it really well.
Compared with the most common FDA audit findings, an auditor found that CRIO’s Electronic Source has safeguards against half. That means fewer deviations for CRIO sites and improved sponsor satisfaction.
Rightly or wrongly, PIs are personally liable for the conduct of the study…. a system that reduces protocol deviations provides protection for PIs.
CRIO’s system saves time on countless tasks that take up a coordinator’s day, from printing and assembling paper binders to completing subject headers. A thorough study showed that CRIO resulted in 25% time savings from paper-based processes.
In the exam room, the system is like an app, not a cumbersome program. It has the look and feel of efficiency, which is what you want.
CRIO’s system can double your clinical trial recruitment effectiveness by increasing your site’s call capacity, tracking patient interactions and organizing campaigns that are tailored to each study. With the one-click call and text capability, your site can achieve four times the response rate.
CRIO has *easily* the best recruitment functionality of any product available. The integration of CTMS, e-source, and recruiting is largely seamless.
