Securely automate the tedious prep work of CDISC data mapping. ClinPilot translates Excel specifications into compliant, production-ready SAS and R candidate code in minutes - accelerate trial programming workflows while keeping your data 100% secure.
Trusted Compliance
Designed to Meet Strict FDA, PMDA, and GxP Validation Requirements | 100% CDISC Compliant
Automating standard specifications can reduce baseline SDTM and ADaM code generation time by up to 60%.
Eliminate manual specification mapping. Our engines reliably translate raw clinical data into CDISC standards with program-ready precision and automated structural derivations.
Deploy intelligent validation agents that automatically ingest guidelines and detect discrepancies across datasets, TLFs, and define.xml.
Secure, role-based web applications tailored for sponsors and biostatisticians to track clinical programming deliverables, monitor validation progress, and manage clinical data assets securely.
Securely drag and drop your clinical Excel specification sheets into ClinPilot.
Let our CDISC-trained mapping engine automatically generate your SAS or R candidate code.
Export precise candidate code, ready for validation within your controlled environment.
We know clinical trial teams are highly protective of their Statistical Computing Environments (SCEs). ClinPilot is built to adapt to your existing processes, not the other way around.
No forced migrations. Generate standardized code that directly exports into your existing, validated SAS or R environment.
ClinPilot respects your development guidelines. The generated code aligns with your team's structural and formatting preferences.
Designed to augment your workflow, not replace it. Accelerate boilerplate generation so your programmers can focus on rigorous QC.
ClinPilot operates on a strict zero-data-retention architecture engineered for the stringent security requirements of clinical trials. Uploaded specification sheets and protocol documents are processed within a secure, ephemeral environment.
Your clinical data and proprietary metadata are never stored, saved, or utilized to train public AI models. All data is encrypted in transit and at rest using industry-standard protocols, ensuring absolute confidentiality.
We recognize that in regulatory submissions, programmatic traceability is non-negotiable. ClinPilot is deliberately designed as a "Human-in-the-Loop" candidate code generator, augmenting rather than replacing your experienced statistical programming team.
The platform accelerates the initial drafting phase by outputting clean, structurally sound SAS or R code. This empowers programmers to bypass tedious mapping boilerplate and immediately transition to rigorous QC and double-programming workflows—preserving your standard operating procedures and FDA/EMA compliance.
Bring your own Excel specifications. Schedule a 30-minute walkthrough where we ingest your data templates and generate compliant candidate code in real-time.