Biostatistical Consulting

Our seasoned biostatisticians and statistical programmers analyse your data throughout your trial to deliver critical insight into every phase of your trial starting with study design.

Our services include:

• Support with design of clinical trials including novel designs across drug development programs and observational studies.
• Writing statistical sections of complex protocols including master protocols
• Sample size and power calculations
• Adaptive trial designs and interim analyses
• Statistical analysis plan
• SAS and R programming 
• Pharmacokinetic analysis and reporting
• Statistical methodologies to handle and prevent missing data.
• Investigator brochures and development safety update reports (DSUR)
• Independent data monitoring committees support