We have experienced biostatisticians and certified SAS programmers who are familiar with CDISC standards. They can provide any of the following services:

• Sample size calculations
• Randomization schedules
• Statistical sections of study protocols
• Study Design
• CRF Design and Review
• Statistical analysis plans
• SAS programming of statistical tables, data listings, and graphs for clinical study reports
• Analysis datasets meeting CDISC standards
• Interim analyses
• Statistical support for Data Monitoring Committees/Data Safety Monitoring Boards
• ISS and ISE analyses
• Post-hoc and exploratory analyses
• Publications support and review
• Statistical support for regulatory meetings
• Statistical consulting and interpretation of results