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