At SITEC Technologies, we offer specialized Clinical SAS (Statistical Analysis System) services to help pharmaceutical, biotechnology, and healthcare organizations manage and analyze clinical trial data with precision, compliance, and efficiency. Our mission is to deliver accurate, audit-ready outputs that meet global regulatory standards while accelerating the clinical research process.

Our highly skilled SAS programmers and biostatisticians work with internationally recognized standards such as CDISC SDTM (Study Data Tabulation Model) and ADaM (Analysis Data Model) to ensure seamless integration, validation, and submission to authorities like the FDA, EMA, and PMDA. We manage the complete statistical programming lifecycle — from data cleaning and transformation to creating detailed tables, listings, and figures (TLFs) for clinical study reports.

Our Clinical SAS service offerings include:

• Clinical trial data management, mapping, and transformation
• SDTM and ADaM dataset creation and validation
• Statistical programming and biostatistical analysis
• TLF generation for regulatory submissions
• Data quality control and compliance checks
• Regulatory-ready documentation and reporting

We combine deep industry expertise, advanced technical skills, and a quality-first approach to ensure accuracy, timeliness, and compliance. Whether you need full-service programming support or specialized consulting, SITEC Technologies provides flexible engagement models to fit your project’s scope and timeline.

Partner with SITEC Technologies for Clinical SAS services that transform raw data into actionable insights, ensure global regulatory compliance, and help bring life-changing treatments to market faster.

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