Clinical Biostatistics Services
Comprehensive biostatistics and programming support for study objectives, endpoints, and reporting requirements.
Integrated Biostatistics
Our biostatistics and programming support connects study objectives, endpoints, estimands, sample size assumptions, analysis methods, data standards, and reporting requirements. Globyz Clinical Solutions coordinates this service in collaboration with CEBIS USA LLC, its U.S. affiliate and clinical research arm. The teams work together within an agreed delivery model, and clinical studies are conducted through CEBIS USA.
Discuss Your Statistical Requirements
Statistical Excellence
Connecting analysis & reporting
Biostatistics Capabilities
Study Design and Statistical Planning
- Protocol and endpoint review
- Sample size and power considerations
- Randomization and analysis population planning where applicable
- Statistical analysis plan development
- Interim analysis and data monitoring support where included
Statistical Programming and Reporting
- Programming specifications and quality control
- Tables, listings, and figures
- Analysis datasets and traceability documentation
- CDISC aligned SDTM and ADaM support where required and within scope
- Results interpretation support for reports and submissions
Transparent Assumptions
The proposal identifies data standards, programming environment, validation approach, mock shell requirements, review cycles, transfer format, and sponsor responsibilities. Statistical conclusions are presented with appropriate assumptions and limitations.
Partner With Globyz
Share the protocol or synopsis, endpoints, study design, sample size assumptions, regulatory audience, data standards, and planned reporting timeline.