Clinical SAS Solutions for Reliable and Regulatory-Compliant Data Analysis

At Xobit Technologies, we offer expert Clinical SAS (Statistical Analysis System) services to support pharmaceutical, biotech, and healthcare organizations in clinical trial data management and analysis. Our experienced SAS programmers and biostatisticians work with global standards like CDISC, SDTM, and ADaM to ensure your clinical data is accurate, validated, and regulatory-compliant. We assist in generating tables, listings, figures (TLFs), and statistical reports required for FDA/EMA submissions. With precision-driven analytics, we help reduce timelines, enhance data quality, and support critical decision-making at every phase of the drug development lifecycle.

Our Clinical SAS team specializes in handling complex datasets from Phase I to Phase IV clinical trials. We provide services including data cleaning, validation, macro programming, statistical modeling, and eSubmission support. Leveraging tools like Base SAS, SAS/STAT, and SAS/Graph, we ensure complete integrity and transparency in your statistical outputs. At Xobit Technologies, we understand the importance of compliance, accuracy, and efficiency in clinical research. Our solutions are designed to help clients meet tight regulatory deadlines while maintaining the highest standards in data integrity, patient safety, and reporting excellence.

Services Core Features

Tailored marketing strategies aligned with your business goals. Competitor analysis and market research for actionable insights. Roadmaps for short-term campaigns and long-term growth. content creation and scheduling for maximum engagement. Community management to interact with your audience.