Our Biostatisticians contribute to the whole process from designing the studies to ensuring enough data and information are collected, analysed and evaluated as well as interpreting the results.

  • Input on study design and endpoints
  • Support, participation and preparation of data for meetings with regulatory authorities
  • Sample size and power calculations
  • Randomisation
  • Statistical analysis plans
  • Input to/review of clinical study protocols and reports, clinical investigational plans and reports
  • Interim analyses
  • Data safety committee (DMC) support
  • Statistical analysis of clinical trial results independent of study design
  • Review of and input on publications as well as assistance in answering editors’ comments

We provide our customers with cost-effective advice, conduct and reporting of clinical trials.