Our business is to capture data, store data and analyze data to support decision-making in health.   We custom-tailor our IT solutions to manage data for clients in government agencies, universities, hospital systems and other groups.  Our major government contract for the past 25 years is from the National Cancer Institute’s Cancer Therapy Evaluation Program, or “CTEP.”  Through CTEP, we have developed innovative software solutions on an enterprise level allowing cancer clinical trials across the United States and internationally to be conducted with increased collaboration across academic medical centers, rapid reporting of adverse events across the system, and reduced time to reach common clinical trial protocols used at multiple centers, to name just some features. We excel at finding just the right informatics solution to meet our client’s needs and we are proud to have received numerous awards from the National Institutes of Health and the National Cancer Institute for our work in improving clinical trial operations through our IT platforms.

CTIS works additionally to help clients modernize their IT infrastructure.  As health systems and healthcare companies work towards their digital transformation, CTIS is a valued and trusted partner.  Our capacities include assisting clients with managing and optimizing critical infrastructure, assisting in migration of datasets to the cloud, conducting data analytics and visualization, and advising on system-wide architecture.   Learn more (this will be a link to Featured Projects)

Our Portfolio

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 to market.

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


CMMI Dev/3

Microsoft Gold Partner


ISO 9001:2015 – Quality Management

ISO 20000:2018 – Service Management

ISO 27001:2013 – Security Management

Scaled Agile Bronze Partner