Clinical Development & Statistical Analysis
Accelerate your clinical trials and research with robust statistical design and execution
Clinical Development & Statistical Analysis
Fueling breakthroughs with Statistical Clarity
- Service: End-to-end statistical support for clinical studies.
- Expertise Applied: Protocol development, sample size calculation, randomization, SAS/R programming for analysis datasets, tables, figures, and listings (TFLs), and statistical analysis plans (SAPs).
- Client Benefit: Reduced trial timelines, regulatory-compliant analysis, and high-quality data interpretation for publications and submissions.
We offer comprehensive statistical support throughout the clinical research lifecycle, from protocol development to reporting.
Applications:
Writing statistical analysis plans (SAPs)
Generating clinical study reports (CSRs)
Preparing regulatory submissions
Risk-based and centralized monitoring strategies
Benefits:
Meet compliance standards (FDA, EMA, ICH) with confidence
Save time with streamlined reporting and clean data pipelines
Enhance trial integrity with robust monitoring and analysis