 i3Cube™ is the first trial and data management system to automate the entire clinical process from beginning to end—allowing for shorter timelines, lower costs, better collaboration, and greater team efficiencies. Created by i3 clinical experts working with technology industry leaders like Adobe®, this next-generation solution is available exclusively from i3.
Here’s why the pharmaceutical, medical device, and biotechnology industries will love i3Cube: Comprehensive integration
i3Cube guides users all the way from site identification and activation to final data delivery in one fully integrated, scalable, easy-to-use tool. Designed for efficiency
i3Cube consolidates software and services in a unique best-of-breed solution to eliminate redundancies, saving both time and money. Superior control
i3Cube's dashboards place real-time data at a user's fingertips from a single online sign-on for more proactive decision making throughout the trial. Automated workflow
i3Cube is a highly adaptable Web 2.0 application that lets sponsors easily configure workflow to increase automation for multiple processes. Unprecedented visibility
i3Cube closely links sponsor, site, and CRO to enhance trial collaboration, track milestones, and improve communication. Enhanced recruitment
i3Cube mines our database of nearly 60,000 investigators to find those with the most appropriate patient populations and identify superior clinical sites. Investigator ease of use
i3Cube’s user-friendly features help reduce investigators’ administrative burden so they can focus on the patient. Strict compliance
i3Cube’s adherence to the highest standards yields an audit-ready, reproducible development methodology designed for our global environment. Major system features currently include: ■ Site identification and management tools
■ Patient enrollment and management
■ Informative dashboards
■ Quick custom and standard reports
■ Essential document management with eTMF
■ Clinical monitoring tools
Future releases include: ■ Data capture (EDC) and query management
■ Ability to link with any IVR
■ Patient safety monitoring
■ Patient-reported outcomes | 
