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
