Investigate's central database architecture with built-in standards and ontology ensures that data elements remain consistent and preserved across clinical trials. Transparent data across the enterprise can be re-purposed across traditional business and functional silos.

Quickly identify potential study cohorts based on demographic, phenotypic, and genotypic criteria.

Investigate includes QueryBuilder™, an intuitive reporting tool that enables researchers to tap into rich data sets intuitively and without knowing the underlying structure or location of the data. Easily generate ad-hoc reports without programming skills.

Use the Workflow Builder's™ drag-and-drop, graphical user interface to build workflows specific to different protocols, studies, and organizations. 

Create participant surveys, data entry elements and screens, and other study forms using the Configure™ tool. Gather rich, specific data sets while binding all data points appropriately to a central ontology.

Customizable dashboards provide easy access to all the important research information resources needed to keep studies moving forward. Survey form libraries, technical protocols, literature, funding information, and news are all displayed on a single screen for quick reference. Investigate also facilitates multi-center collaboration through shared tasks, calendars, toolsets, protocols, and best practices.  

Security services guarantee role-based access control and HIPAA compliance. Access to research data is controlled at the database, transaction, and application levels, making use of reliable de-identification services. All components of the Investigate suite comply with the regulations set forth under HIPAA and 21 CFR Part 11 as required for FDA-regulated research. Specifically, Investigate supports automatic logout, audit trials, limited access, date/time stamping, and other external security safeguards.