Our clinical programming team is the largest department within our organization. We work closely with biostatisticians to make sure the programs are developed as per the statistical goal of the study.

Our biostatisticians work with clients to determine methods for collecting, analyzing and presenting data while maintaining compliance with regulatory guidelines. Our programmers create programs to meet your needs and produce meaningful statistical tables and reports.

Our clinical programming team consists of SAS Base and Advanced Certified individuals with thorough knowledge of all the clinical phases and therapeutic areas across the drug development spectrum making them an ideal fit within the existing project teams.

Our Clinical Programming Services

Advanced SAS Macro programming

SAS Integrations with Medidata RAVE/Oracle InForm

Generation of Tables, Figures and Listings

Production of Interim Analysis and ISS/ISE Reporting

Creation of CDISC documentation (define.xml)

Creating global level SAS Utilities

Our SAS Solutions Expertise

SAS Life Science Analytics Framework

Formerly known as SAS Drug Development (SDD). We expertise in migration and developing custom integrations using SDD API and automation of SAS processes.

SAS Clinical Trial Data Transparency

SAS Clinical Trial Data Transparency provides researchers with a globally available, secure clinical trials data repository with easy access to SAS Analytics for valid research purposes.

SAS Clinical Data Integration

SAS Clinical Data Integration (CDI) is built on top of SAS Data Integration Studio with a clinical plugin for CDISC standards. It allows you to manage the standards and automate the mapping process.

SAS Enterprise Grid

SAS Enterprise Grid is an analytic computing environment that provides high availability and accelerates processing. SAS computing infrastructure is distributed in Grid Nodes, flexible to grow over time as users/data increases.

Our team of highly experienced SAS programmers are ready to start working on your project.