Clinical trial planning, design, and analysis

PHASTAR can support the planning, design and analysis of your clinical trial programme. Regardless of the complexity of your project, PHASTAR can provide expert statistical solutions and experienced technical advice, tailored to meet your needs.

Our services include

  • Statistical input into study design & 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
  • 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

Independent data monitoring committees

PHASTAR offers sponsors seamless support for Independent Data Monitoring Committees, through expert advice and support, agile and adaptable approach to systems and logistical expertise.

For more information on IDMCs click here.

Learn more about our services