Products
ClinicalStudyReports
From Protocol + SAP to complete CSR in seconds. Automate the most time-consuming parts of your regulatory submissions with AI that delivers 100% reproducible, fully traceable outputs.
How it works
Non-Data Section Drafting
Input your Clinical Protocol and Statistical Analysis Plan (SAP). Ritivel instantly drafts all non-data sections of your CSR within seconds.
- 1Takes Clinical Protocol as input
- 2Takes SAP (Statistical Analysis Plan) as input
- 3Generates non-data sections instantly
Biostatistical Analysis
Post data lock-in, Ritivel performs automatic biostatistical analysis and generates Tables, Listings, and Figures (TLF).
- 1Automatic analysis post data lock-in
- 2Generates Tables, Listings, Figures (TLF)
- 3Fully traceable to source data
Data-Centric CSR Generation
TLF outputs are converted into the data-centric sections of your CSR, completing the full document with end-to-end traceability.
- 1Converts TLF to narrative sections
- 2Complete CSR document
- 3Word-level traceability maintained
Why choose Ritivel for CSRs
Seconds, Not Weeks
Draft complete CSRs in seconds instead of weeks of manual work.
100% Reproducible
Same input always produces the same output. Critical for regulatory compliance.
Word-Level Traceability
Every word, number, and sentence traceable back to source documents.
Ready to transform your CSR workflow?
See how Ritivel can help your team deliver CSRs faster with complete traceability.