Biostatistics
At Clinovo, we are able to provide sponsors with hands-on support to clinical projects across multiple therapeutic areas. All our biostatisticians, as well as clinical and statistical SAS® programmers have Masters or PhD degrees. They have worked on a broad range of therapeutic areas for several leading biotech companies throughout the Silicon Valley. Our senior biostatistics team members have an average of 20 years experience in both clinical data management and statistical SAS® programming. All SAS® programmers have acquired the SAS® certification delivered by the SAS® Institute. We provide clinical research professionals with:
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Our comprehensive range of biostatistics services covers any clinical trial phase and therapeutic area:
- Clinical and Statistical SAS® programming
- Statistical Analysis Plan (SAP)
- Sample Size and Power Calculation
- Randomization Schedules & Implementation
- Statistical CRF and Database Review
- CDISC® Study Data Tabulation Model (SDTM) Mapping & Conversion
- Analysis Dataset Programming and Documentation
- Tables, Listings and Figures Validation and Quality Control
- Interim Analysis
- Patient Profiles
- Physician Reports
- ISS/ISE Preparation
- Ad hoc Statistical Support
- DSMB/SMC/DMC Participation
- Statistical Representative at FDA Pre- and Post-Submission Meetings
- Standard Programming and Reporting Catalog (SPARC)
- Data Integration
- Tables, Listings and Figures Programming
