At N.V.DATA SYSTEMS, we provide comprehensive Clinical SAS (Statistical Analysis System) services designed to support the entire clinical trial data lifecycle — from data management and statistical analysis to reporting and regulatory submission. Our goal is to empower pharmaceutical, biotech, and healthcare organizations with accurate, compliant, and timely insights that drive better decision-making.

Our team of certified SAS programmers and biostatisticians brings deep expertise in CDISC standards, including SDTM, ADaM, and Define-XML, ensuring compliance with FDA and EMA submission requirements. We specialize in transforming complex clinical data into well-structured, analysis-ready datasets and generating precise TLF (Tables, Listings, and Figures) outputs that meet the highest quality standards.

By leveraging automation, validation tools, and robust quality control processes, we help accelerate trial timelines, minimize errors, and maintain full traceability throughout the data flow.

Whether you need end-to-end SAS programming, statistical reporting, or submission package preparation, N.V.DATA SYSTEMS delivers reliable, cost-effective solutions tailored to your study needs — enabling faster regulatory approval and confident, data-driven outcomes in clinical research.