Clinical Research IO (CRIO)

Clinical Research IO (CRIO) is dedicated to transforming the clinical research landscape for our customers, which include pharma companies, biotech firms, research sites, and academic research centers. These organizations often face significant challenges in managing regulatory workflows, ensuring data accuracy, and maintaining compliance, traditionally burdened by paper-based processes and manual data entry. This is why CRIO developed an intuitive eSource solution designed to capture data directly at the point of patient interaction. Our system lightens the operational load on research sites and significantly drives protocol compliance from the outset.

Our customers need reliable, protocol-driven data but are frequently bogged down with administrative details and manual tasks that divert focus from quality. CRIO addresses this by offering a powerfully integrated suite of tools including eSource, CTMS (Clinical Trial Management System), eRegulatory, and stipend solutions. This comprehensive platform streamlines operations, allowing for remote monitoring and real-time data review, which is crucial for timely decision-making and oversight. By eliminating up to 90% of paper and improving data quality by as much as 80%, we help our customers reduce errors, save time, and lower the risk of protocol deviations and FDA audit findings. CRIO's system is built by clinical research experts who understand the critical needs of research sites, ensuring that our configurable and scalable templates standardize data capture, while our connected ecosystem supports all essential data collection activities, making trials run seamlessly and efficiently. We empower our customers to focus on what truly matters: advancing medical science and improving patient outcomes by providing a digital-first, site-centric approach that delivers unique value and faster timelines.