March 9th, 2010
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TII Informatix Group
Post Market Surveillance, Outcomes Research and Data Management Services for Healthcare
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Biostatistics

The TII statistics group is involved throughout the life of a project—including study design, development of study materials, data summary reporting, statistical analysis, and publication—to ensure that each project is grounded in sound statistical methods. Our approach to statistical support is to work closely with the client, identifying specific analysis needs. Whether the needs involve statistical programming, interim analyses, data summaries, final analyses, or statistical writing, we are committed to working with you to provide a quality product.

We provide the following biostatistical services in support of your clinical trials on a routine basis:

  • Study design
  • Sample size calculations
  • Protocol review and consulting
  • CRF review
  • Randomization
  • SAS® programming (PC SASR v9.1)
  • Audited tables, figures and listings
  • Interim and final analyses
  • Statistical reporting
  • Clinical study report review
  • Common technical document support
  • Data Monitoring Committee (DMC) support
  • Regulatory agency support and interaction including

    • FDA
    • EMAA
    • and other regulatory agencies
  • Annual safety updates
  • Consulting and training
  • Database integration for integrated summaries (CTD, NDA)

Why Us

In March 2008 TII was named a finalist for the Greater Richmond Technology Council (GRTC) IT Builders Award. This award is presented to the information technology services provider that demonstrates an outstanding ability to deliver technology-enabled business transformation solutions to either its internal or external clients.


Contact Us

  • Call us today at 1-888-727-8667 or click here to request information on how TII Informatix can deliver innovative and custom clinical solutions for your business.

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