At Infosavant Technologies, we provide specialized Clinical SAS (Statistical Analysis System) services to support pharmaceutical, biotechnology, and healthcare organizations in managing, analyzing, and reporting clinical trial data with precision and compliance. Our goal is to help you transform raw clinical data into accurate, audit-ready insights that meet global regulatory requirements.

Our team of expert SAS programmers and biostatisticians follows industry best practices and standards such as CDISC SDTM (Study Data Tabulation Model) and ADaM (Analysis Data Model) to ensure seamless integration and submission to regulatory bodies including the FDA, EMA, and PMDA. We handle the full spectrum of statistical programming, from data cleaning and transformation to generating high-quality tables, listings, and figures (TLFs) for clinical study reports.

Our Clinical SAS service portfolio includes:

• End-to-end clinical trial data management and transformation
• SDTM and ADaM dataset creation, mapping, and validation
• Statistical programming and advanced data analysis
• TLF generation for regulatory submissions
• Data integration, validation, and quality control
• Compliance with global regulatory guidelines and audit readiness

We combine deep domain knowledge, technical expertise, and a quality-driven approach to deliver reliable, timely, and compliant solutions. Whether you require complete statistical programming support or specialized SAS consulting, we tailor our engagement to your project’s scale and timelines.

Partner with Infosavant Technologies for Clinical SAS services that accelerate submissions, ensure data integrity, and bring life-changing treatments to market faster.