What We Can Do

  • Software development and licensing for the design and analysis of adaptive and other complex clinical trials
  • Consultation including protocol and statistical analysis plan review
  • Representation at regulatory and advisory committee meetings
  • Management of and representation at data safety monitoring boards
  • Development and validation of scales used in clinical trials
Man typing on computer with charts

Introducing S.M.A.R.T.™

  • Sequential Monitoring of Clinical Trials
  • Multiple Endpoints: Design and Analysis of Clinical Trials with Multiple Endpoints
  • Adaptive Clinical Trials
  • Response Predictive Analytics
  • Time Driven Interim Analyses

What is Unique About Our Software?

Most statistical calculations rely on approximations for planning and analyzing clinical trials. S.M.A.R.T.™ is using a cutting-edge methodology that provides the exact solutions for clinical trial designs. Our methodologies, published in leading statistical journals, ensure their advantage over traditional approaches.

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