Clinical SAS Services

Transform Clinical Data into Reliable Regulatory Insights

Clinical SAS is widely used in the pharmaceutical, biotechnology, and healthcare industries for managing, analyzing, and reporting clinical trial data. Our Clinical SAS services support clinical data processing, statistical analysis, reporting, and submission-ready deliverables while helping organizations maintain consistency, quality, and traceability throughout the clinical development lifecycle.

Our Clinical SAS Services

• Clinical Data Management Support – Process, validate, and organize clinical trial datasets for analysis and reporting.
• SAS Programming – Develop validated SAS programs for clinical data processing, analysis, and reporting.
• CDISC Implementation – Support standardized clinical data structures such as SDTM and ADaM.
• SDTM Programming – Transform clinical trial data into standardized SDTM domains.
• ADaM Programming – Create analysis-ready datasets based on clinical study requirements.
• TLF Development – Develop Tables, Listings, and Figures for clinical study reports.
• Statistical Programming – Perform statistical analyses and generate study outputs using SAS.
• Data Validation – Perform independent programming and quality checks to improve data accuracy and consistency.
• Regulatory Submission Support – Prepare standardized datasets and documentation for regulatory submissions.
• SAS Maintenance & Support – Maintain, optimize, and update clinical SAS programs and reporting workflows.

SAS Base

Core SAS programming environment used for data manipulation, analysis, reporting, and automation.

SAS Macro

SAS macro language helps programmers create reusable code and automate repetitive clinical programming tasks.

SAS SQL

Used to query, join, filter, transform, and manage clinical datasets efficiently.

SAS/STAT

Provides statistical procedures for analyzing clinical and research data.

SAS/GRAPH

Used to create graphical representations and visualizations from clinical and statistical data.

SAS ODS

Output Delivery System (ODS) generates clinical reports and outputs in formats such as PDF, RTF, HTML, and other supported formats.

SAS Enterprise Guide

User-friendly SAS interface for data access, analysis, reporting, and workflow development.

SAS Studio

Web-based SAS development environment for writing, running, managing, and sharing SAS programs.

SAS Viya

Modern analytics platform supporting statistical analysis, data management, AI, machine learning, and cloud-based analytics.

CDISC SDTM

Study Data Tabulation Model (SDTM) provides standardized structures for organizing clinical trial tabulation data.

CDISC ADaM

Analysis Data Model (ADaM) provides standardized analysis datasets designed to support statistical analysis and traceability.

CDISC Controlled Terminology

Standard terminology used to improve consistency and interoperability of clinical trial data.

Clinical SAS Programming Areas

• SDTM Programming Convert collected clinical trial data into standardized SDTM domains such as DM, AE, CM, EX, LB, VS, and MH.
• ADaM Programming Develop analysis-ready datasets such as ADSL and other study-specific analysis datasets.
• TLF Programming Create statistical Tables, Listings, and Figures based on approved specifications.
• QC & Validation Perform independent validation, comparison, and quality checks of datasets and clinical outputs.
• Metadata & Documentation Maintain specifications, define.xml-related metadata, dataset documentation, and programming documentation as required.