At BMS Infosolution Software Technology, we provide specialized Clinical SAS (Statistical Analysis System) services that support pharmaceutical, biotech, and healthcare organizations in conducting regulatory-compliant clinical trials. Our team of SAS-certified professionals ensures accurate statistical analysis, data management, and reporting for all phases of clinical research.
We assist in transforming complex clinical data into meaningful insights using industry-standard SAS tools and methodologies. From data cleaning, validation, and transformation to generating TLFs (Tables, Listings, and Figures), we deliver high-quality results that meet FDA, CDISC, and ICH guidelines. Our solutions help reduce trial timelines and improve regulatory submission success rates.
Whether you are conducting Phase I-IV trials or post-marketing surveillance, BMS Infosolution provides end-to-end support with clinical programming, statistical modeling, and real-time reporting dashboards. Our services empower CROs, sponsors, and life science companies to make confident, data-driven decisions with precision and compliance.
End-to-End Clinical Data Analysis – Comprehensive support from data collection to submission-ready outputs.CDISC Compliance (SDTM & ADaM) – Structured and standardized data formats for regulatory acceptance.SAS Programming for TLFs – Automated generation of accurate and customizable tables, listings, and figures.Regulatory-Ready Reporting – Reports aligned with FDA, EMA, and ICH guidelines for smooth approvals.Secure Data Handling – HIPAA-compliant data security and quality control practices to protect sensitive health data.