Our development process emphasizes scalability, performance, and cybersecurity from day one. Leveraging cloud-native architectures, DevOps practices, and Big Data analytics integration, we ensure that every application we build is secure, high-performing, and ready to scale as your business grows. With dedicated testing & QA practices in place, every product undergoes rigorous validation to ensure quality, compliance, and optimal user experience. At SNS Datatac Solutions, we don’t just develop software—we deliver digital transformation.
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At SNS DATATAC SOLUTIONS, our Clinical SAS capabilities are engineered to bring efficiency and accuracy across the entire clinical research lifecycle. We provide advanced statistical programming and data management solutions tailored for pharmaceutical, biotech, and CRO partners. By leveraging our deep domain knowledge in SAS and clinical regulations, we help teams produce high-quality datasets and submission-ready outputs that meet stringent global standards such as CDISC, SDTM, and ADaM.
What sets us apart is our ability to build scalable and reusable programming frameworks that reduce development time while ensuring compliance and traceability. Our Clinical SAS experts work closely with biostatisticians and clinical teams to automate TLF (Tables, Listings, and Figures) generation, perform complex statistical analyses, and clean data with full audit trails. This leads to faster study completion, better resource allocation, and a smoother path toward regulatory submission.
SNS DATATAC SOLUTIONS empowers sponsors to make faster, data-driven decisions through timely insights generated from clinical trials. From early-phase studies to large-scale multi-center trials, we implement validated SAS solutions that integrate seamlessly with clinical data systems. Our proactive quality checks, consistency reviews, and real-time programming support reduce downstream risks and drive overall trial success with transparency and confidence.
Tailored SAS macros and reusable code libraries designed to meet study-specific requirements, reducing turnaround time and increasing efficiency.
Rapid generation of high-quality TLFs and listings to support real-time data review, enabling faster decision-making during trials.
Seamless alignment with global regulatory standards (FDA, EMA) through built-in checks, traceability, and structured data submissions.
Full visibility from raw data to final analysis outputs, ensuring data integrity and simplifying audits and inspections.
SAS solutions that scale from early-phase exploratory trials to late-phase pivotal studies, providing consistent performance across trial stages.
Rigorous internal QC processes and dual programming approaches to ensure accurate, validated, and reproducible outputs.
SNS DATATAC SOLUTIONS delivers accurate, compliant analytics for clinical trials. We turn complex trial data into clear, actionable insights.
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