Clinical Trial Data Analysis with SAS
We combine deep industry expertise, strong technical proficiency, and a quality-driven approach to ensure accurate, timely, and compliant deliverables.
At Infinext Technologies, we deliver specialized Clinical SAS (Statistical Analysis System) services designed to help pharmaceutical, biotechnology, and healthcare organizations manage, analyze, and report clinical trial data with accuracy, compliance, and efficiency. Our goal is to transform raw clinical data into meaningful insights that support faster, more informed decision-making and regulatory approvals.
Our experienced SAS programmers and biostatisticians work in compliance with global industry standards such as CDISC SDTM (Study Data Tabulation Model) and ADaM (Analysis Data Model), ensuring seamless integration and submission to regulatory authorities like the FDA, EMA, and PMDA. We manage the full statistical programming lifecycle — from data cleaning and transformation to generating detailed tables, listings, and figures (TLFs) for clinical study reports.
Our Clinical SAS service capabilities include:
- End-to-end clinical trial data management and transformation
- SDTM and ADaM dataset creation, mapping, and validation
- Statistical programming and biostatistical analysis
- TLF generation for regulatory submissions
- Data validation, quality control, and compliance checks
- Regulatory-ready documentation and reporting
We combine deep industry expertise, strong technical proficiency, and a quality-driven approach to ensure accurate, timely, and compliant deliverables. Whether you need complete end-to-end statistical programming or targeted consulting services, Infinext Technologies provides flexible engagement models tailored to your project’s scale and timelines.
Partner with Infinext Technologies for Clinical SAS services that accelerate submissions, ensure data integrity, and help bring innovative healthcare solutions to market faster.