From single-study validation to enterprise-grade submission readiness. Every plan includes our 8 universal QC bug classes and audit-ready reporting.
Everything you need to know about ClinAssist pricing and plans
A study is defined as a single clinical trial protocol (e.g., a Phase III study with one SAP). Each study gets its own isolated workspace, ADaM/SDTM datasets, and QC configuration. You can upgrade or cancel per study — no cross-study lock-in.
Yes. Book a demo and we'll run ClinAssist on one of your real TLF outputs — live. You'll see exactly what bugs it catches before you commit to anything. No credit card, no obligation.
Absolutely. Upgrade from Starter to Professional mid-study if you need R replication or unlimited tables. Downgrade between studies. All your audit trails and settings carry forward.
ClinAssist independently reproduces your SAS tables in R using haven, dplyr, and rtables. Every cell is compared — counts, percentages, sort order, and formatting. This satisfies FDA's expectation for independent QC without hiring a second programmer.
All processing happens in isolated, encrypted workspaces. We are 21 CFR Part 11 compliant with full audit trails. Enterprise customers can deploy on-premises or in their own VPC. Data is never used for training or shared across customers.
Enterprise plan includes custom rule authoring — write your own checks in Python or R, or have our team build them for you. Professional users can request new check types which we often roll into the core product.
See ClinAssist catch bugs your manual QC is missing. Book a 15-minute demo with real TLF data.