Our Department of Statistics offers many years of extensive experience in handling all statistical tasks, from clinical pharmacology trials to pivotal phase III trials and beyond e.g.:
- Choice of trial design and power calculations
- Input to trial protocols
- Writing of statistical analysis plan
- Establishing and conducting DMCs (Data Monitoring Committees)
- Statistical reports or input to integrated clinical trial reports
- Statistical programming at the expert level
- Insourcing of experienced biostatisticians and statistical programmers
- Interim analyses and meta-analyses
- Statistical input to publications
- Statistical support regarding regulatory issues, at meetings etc.
Our statistical team offers many years of extensive experience in all statistical tasks.
See our core services and bespoke solutions here