Ritivel

Founded by Pavan Kalyan in 2024

AI-native platform for Life-Sciences Documentation

Cost

Demo

Rating

★ People love it

Time to value

Moderate Setup (1-3 hours)

You can use Ritivel to draft regulatory documents like Clinical Study Reports, IND submissions, and CTD modules for pharmaceutical companies. The AI system provides word-level traceability, meaning every statement can be traced back to its source document. You can generate complete CSRs from protocols and statistical analysis plans, automate literature searches, and create Module 2 summaries with cross-references. The system deploys locally on your infrastructure to maintain data security and compliance. It's specifically trained on medical and regulatory language to reduce errors in high-stakes submissions.

What Ritivel does

Convert protocols and SAPs into complete CSRsTrace every document statement to source materialsSearch regulatory guidelines for specific requirementsGenerate literature summaries from PubMed searchesCreate cross-referenced CTD module sectionsDraft nonclinical study reports with AI assistanceAutomate table and figure generation from dataMaintain consistent narrative across document versionsWord-level traceability for every statement100% local deployment with no cloud storageDomain-specific training on medical terminologyGenerates complete CSRs from protocol inputsAuto-generates tables, listings, and figuresLiterature search integration with PubMedCross-reference automation for CTD modulesAir-gapped deployment capability

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