OADA IT SERVICES is a forward-thinking software development company committed to delivering cutting-edge digital solutions that empower businesses.

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Clinical SAS

At OADA IT SERVICES, we provide expert Clinical SAS (Statistical Analysis System) services to support clinical trials and regulatory submissions in the pharmaceutical, biotech, and healthcare industries. Our team of certified SAS programmers and clinical data experts ensures accurate data analysis, reporting, and compliance with global standards like CDISC, FDA, and ICH. We help organizations manage large volumes of clinical data efficiently, transforming raw datasets into actionable insights that drive faster, evidence-based decisions.

From data integration to statistical analysis and report generation, our Clinical SAS services cover the complete data lifecycle. We support Phase I–IV trials, pharmacovigilance, and real-world evidence studies with high accuracy, scalability, and confidentiality. Our flexible delivery models and domain expertise ensure timely results, regulatory readiness, and data-driven clinical success.

We create validated SAS programs to analyze clinical trial data, perform statistical modeling, and generate tables, listings, and figures (TLFs) for clinical study reports.

We ensure compliance with CDISC standards by transforming clinical data into SDTM (Study Data Tabulation Model) and ADaM (Analysis Data Model) formats for FDA submissions.

Our experts handle raw clinical data cleaning, validation, and integration across EDC systems, labs, and third-party sources to ensure accuracy and consistency.

We prepare regulatory-ready outputs, including define.xml, annotated CRFs, and reviewer guides, to support electronic submissions to regulatory authorities like the FDA and EMA.