Biostatistics

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