Clinical SAS
At Scanfii Software Technologies, we provide advanced Clinical SAS (Statistical Analysis System) services to support pharmaceutical, biotechnology, and clinical research organizations in managing and analyzing clinical trial data. Our Clinical SAS experts specialize in creating high-quality datasets, performing statistical analysis, and generating regulatory-compliant reports in accordance with CDISC standards like SDTM, ADaM, and TLFs. We help streamline the clinical data lifecycle to ensure faster, safer, and more effective drug development.
Our solutions are tailored to meet FDA, EMA, and other global regulatory requirements. By leveraging the power of SAS tools and best practices, we ensure accuracy, traceability, and reproducibility of clinical data. Whether you’re running Phase I-IV trials or working on submissions, our Clinical SAS services provide the technical depth and domain knowledge needed to support successful outcomes.
- Regulatory-Compliant Data Standards: Expertise in CDISC standards (SDTM, ADaM, Define.XML) and generation of FDA/EMA-ready submission packages.
- End-to-End Clinical Data Programming: Programming of raw and derived datasets, TLFs (Tables, Listings, and Figures), and validation for clinical studies.
- Statistical Analysis & Reporting: Accurate and efficient SAS-based analysis to support clinical study reports, interim analyses, and regulatory submissions.
