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Ritivel is a Compliance & Audit tool that automates regulatory document drafting for life sciences. It drafts Clinical Study Reports and CTD modules in minutes with word-level traceability.
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About
Ritivel is an AI-native regulatory platform designed for the life sciences industry, including Pharma, Biotech, Medtech, and CROs. It automates the drafting of critical regulatory submissions like Clinical Study Reports (CSRs) and CTD modules, significantly reducing the time from weeks to minutes. The platform ensures 100% reproducibility and offers word-level traceability, allowing users to instantly identify the source of every statement. Ritivel's AI is specifically trained on life sciences and regulatory content, ensuring accuracy and consistency in domain-specific terminology. A key differentiator is its commitment to data security, offering 100% local deployment with no cloud storage, ensuring sensitive data remains within the user's infrastructure and is never used for model training.
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Not publicly disclosed. Check ritivel.com for current pricing.
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