Aligning the Art & Science of Clinical Research® is not just our tagline;
it represents our signature, collaborative approach.


MedTrials is focused on providing biostatistical support through efficient study design, statistical methods development and a thorough understanding of the analytical complexities which is critical to effectively interpret the study outcomes. MedTrials provides comprehensive data analysis and reporting suitable for your regulatory submissions, presentations, and publications.

MedTrials biostatisticians are industry experienced and have a strong knowledge of the industry in a wide variety of therapeutic disciplines. Our diversity of experience, based on sound statistical theory and current scientific knowledge, leads to a clear and accurate picture of your product’s unique characteristics. Careful biometric planning and execution promotes impartial yet compelling evidence-based solutions from valid, reliable, and well-represented data.

Services include:

  • Protocol design and development
  • Sample size estimation and power calculations
  • Statistical analysis plan (SAP) development
  • Randomization
  • Interim and final data analysis
  • Statistical consulting
  • Statistical report writing
  • Statistical SAS programming of tables, listings, and figures/graphs
  • Statistical support for preparation of abstracts, manuscripts, and presentations
  • Meta-analysis, data mining, and exploratory analysis
  • Data Monitoring Committee (DMC)/Data Safety and Monitoring Board (DSMB) participation