Leading the evolution of informatics and health research

The resources necessary to develop and research a single drug can be astronomical—both in terms of time and price. At CTIS, we recognize that advances in medicine require health research to be more efficient, cost-effective, and yield high-quality results. Our portfolio of health IT solutions stems from decades of partnership with clinical trial and research stakeholders.

CTIS is a national leader, developing web-based capture, reporting, and monitoring solutions including ontology-powered analytics tools. Our services help to provide new insight into data—allowing researchers to effectively design and conduct their studies, thereby reducing the time to bring products to market. We also help our clients to improve regulatory compliance and manage quality so that research and operations are more efficient and productivity is enhanced.

The result? We reduce the time it takes to bring life-changing drugs

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  • Trial Conduct
    • Protocol change management
    • Protocol performance monitor
    • Drug management and delivery
  • Trial Reporting
    • Research outcome analyzer
    • Research dashboard monitor
    • Site monitoring and auditing
    • Expedited and non-expedited adverse event reporting
    • E-submissions to FDA
  • Trial Planning
    • Protocol development
    • IRB management
    • Networks and site data interchange
    • Patient accrual
    • Data abstraction
  • Trial Activation
    • CRF designer
    • Regulatory support
    • Clinical development planner
    • Site, patient and investigator registration
    • Electronic IND and NDA submission


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