Statistical programming
Turning raw data into
regulatory-ready insights
The Data Structuring Paradox:
Turning Complexity into Clarity
Clinical data isn’t just collected—it’s structured, standardized, and analyzed to drive regulatory decisions. At Rho, our statistical programming team transforms complex datasets into submission-ready outputs, ensuring accuracy, compliance, and clarity. Whether supporting adaptive trial designs, generating CDISC-compliant datasets, or preparing for regulatory submission, we bring precision to every dataset.
Why Rho?
Why Rho?
Expert CDISC implementation
SDTM and ADaM dataset preparation for seamless regulatory submissions.
Regulatory-ready programming
ISS, ISE, and submission outputs that meet global agency expectations.
Adaptive trial programming
Supporting complex study designs with flexible, scalable coding solutions.
Quality-focused automation
Streamlining processes to improve efficiency and reduce error potential.
Comprehensive statistical
programming support
We provide full-service programming solutions to support clinical research and regulatory success:
CDISC standards implementation
Ensuring compliance with SDTM, ADaM, and Define.xml standards.
Regulatory submissions and reporting
Preparing datasets, tables, listings, and figures for FDA, EMA, and global agencies.
Integrated safety and efficacy analyses
Supporting ISS and ISE for seamless regulatory reviews.
Custom reporting and visualization tools
Enabling data-driven decision-making with clear insights.
Audit and submission readiness
Ensuring datasets are accurate, validated, and submission-ready.
Related insights & resources
Ready to power your trial with expert programming?
Data is only as valuable as the insights it provides. Let’s turn complexity into clarity.
