Contract research organization (CRO) i3 launched a new web-based clinical trial and data management program that will replace the need for multiple systems and applications to manage study activities.
The new technology, i3Cube, centralizes study information into a single location throughout the entire clinical trial process, providing sponsors and investigative site staff with real-time reporting and access to study information. The study team can access the information at any time by logging into a secure web portal.
According to a company release, i3Cube accelerates the data management process by streamlining communication across the entire study team, automating workflow and providing an integrated study library with version control, including an electronic trial master file.
“i3Cube was designed to provide our clients and clinical investigators with a simple, easy-to-use, and streamlined experience,” said i3 CEO Glenn Bilawsky in an i3 statement. “We brought together our use of proprietary health care claims data with our clinical research expertise and developed i3Cube to create time and cost efficiencies for our customers.”