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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
- 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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