We provide comprehensive statistical analysis and reporting services
to address all phases of clinical research and development.
UBC biostatisticians support protocol designs, regulatory
submissions, and provide statistical methodologies for specific
studies and research programs.
Our services include:
- Study Design & Protocol Development – Sample Size/Power
- CRF Design
- Endpoint Selection & Validation
- Statistical Analysis Plans
- Programming
- Randomization schedules
- Data Monitoring Committees
- Clinical Study & Statistical Reports
- Custom Tables, Listings & Figures
- Legacy Database Integration
- Dataset Submission Based on CDISC Guidelines
- Database and SAS Program Documentation
- Medical Writing – application summaries, integrated
summaries
- Regulatory submissions – updates to NDA and sNDA
- Economic Modeling
