Statistical Analysis
Let's collaborate to bring breakthrough treatments to light with your team
ADI can effortlessly support any study for which you need additional help or knowledge to fulfill your regulatory approval deadlines with deliveries that are ready for submission.
Our skilled programmers are a perfect match for current project teams at client sites since they comprehensively understand all phases and have expertise in a wide range of therapeutic areas throughout the drug development spectrum.
Our team of professionals is acquainted with CDISC and can put together a CDISC strategy that meets organizational, monetary, and regulatory targets. We have created datasets for several SDTM, ADaM, and CDISC-compatible studies and completed numerous CDISC-compliant regulatory filings.

Our expertise entails
- SAS programming
- Macro production, validation, and optimization
- Interim analysis support
- CDISC mapping/conversion capabilities
- CDISC submission-ready dataset development and QC for submission compliance
- Analysis datasets and TLFs development
- Define.xml files for SDTM and ADaM
- Submission-ready packages (Define XML, Reviewer’s Guide & Analysis Metadata)