Statistical Consulting

PHASTAR can support the planning, design and analysis of your clinical trial programme.

We offer the following services:

  • Statistical input into study design and protocol development
  • Adaptive study designs
  • Sample size calculations
  • Analysis plans
  • Optimising study success
  • Identifying the primary endpoint
  • Modelling and simulation
  • Prediction of drug exposure
  • Optimal evaluation of information for on-going clinical trials (interim analyses, sequential trial monitoring)
  • Independent data monitoring committees
  • Setting up randomisation schemes
  • Multiplicity (optimally evaluate more than one outcome in a trial)
  • Regulatory advice
  • Observational and epidemiological studies
  • Interpretation of results
  • Data visualisation
  • Statistical training

Regardless of the complexity of your project, PHASTAR are able to provide statistical solutions and expertise.