Statistics

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