Core Therapeutic Specialization
[01]
Oncology Clinical Trials
Specialized programming for complex oncology protocols, ensuring rigorous data integrity and adherence to global regulatory standards.
[02]
CDISC Standards, SDTM, & ADaM
Expert implementation of SDTM and ADaM standards to ensure seamless data transfer and global regulatory compliance for oncology data.
[03]
Statistical Analysis & Reporting
Comprehensive support for statistical analysis and clinical reporting, delivering high-quality data for mid-size CROs and global sponsors.
THE SIRIX ADVANTAGE
Quality-First Data Engineering
We deliver systematic precision in clinical SAS programming, specifically tailored for the complex demands of oncology clinical trials. Our team brings deep expertise in CDISC standards and SDTM/ADaM, ensuring that every data management step meets the highest regulatory benchmarks for mid-size CROs.
THE SIRIX ADVANTAGE
Clinical Judgement, Not just code
Our team is mix of medical doctors and certified clinical trials programmers. That combination shapes how protocols, endpoints, and adverse event patterns get read — not just programmed to spec. It's the difference between data that passes QC and data that holds up under a reviewer who understands the disease
THE SIRIX ADVANTAGE
Depth Where Others OutsourceÂ
Informative censoring, competing risks, multi-covariate hazard models — the analyses most generalist SAS teams avoid or hand off. We build IPCW-adjusted and two-stage Cox models for PFS sensitivity analysis, and RECIST 1.1-based response derivation, as core work, not a specialty request.
THE SIRIX ADVANTAGE
Regulatory Experience, Not Just Trial Support
FDA and PMDA BLA submission work across OS, PFS, ORR, and TTD endpoints — plus early, hands-on experience with BIMO3/CLINSITE, CDISC's newly introduced site-level dataset. Submission-side experience, not just dataset delivery.
We empower small to mid-size CROs with systematic precision in clinical SAS programming and oncology data management, ensuring every trial meets the highest international standards.
At Sirix Informatics, we bridge the gap between complex oncology data and regulatory clarity. Our mission is to provide mid-size CROs with the technical precision and clinical expertise required to navigate the rigorous demands of modern clinical trials.
