End-to-End Clinical SAS Solutions
At United Wireless Technologies, we provide specialized Clinical SAS (Statistical Analysis System) services to support pharmaceutical, biotechnology, and healthcare organizations in their clinical research and regulatory submission processes. Our expertise lies in transforming complex clinical trial data into accurate, compliant, and meaningful insights that drive informed decision-making.
Our team of certified Clinical SAS programmers and biostatisticians work with global industry standards, including CDISC SDTM (Study Data Tabulation Model) and ADaM (Analysis Data Model), ensuring regulatory compliance with authorities such as the FDA and EMA. We handle the complete statistical programming lifecycle, from data cleaning and validation to generating high-quality tables, listings, and figures (TLFs) for clinical study reports.
Our Clinical SAS service offerings include:
- Clinical trial data management and transformation
- SDTM and ADaM dataset creation and validation
- Statistical programming and biostatistical analysis
- TLF generation for regulatory submissions
- Data integration and quality control
- Compliance with global regulatory standards (FDA, EMA, PMDA)
We combine technical expertise, domain knowledge, and a quality-driven approach to deliver precise, timely, and audit-ready outputs. Whether you need end-to-end support or targeted SAS programming assistance, our flexible engagement models ensure that your project requirements are met efficiently.
With United Wireless Technologies as your Clinical SAS partner, you gain a trusted ally in achieving faster submissions, higher data accuracy, and full compliance — helping you bring new treatments to market with confidence.