Ritivel builds AI software for life sciences regulatory teams handling clinical and submission documents. Its products generate clinical study reports, Common Technical Document summaries, and regulatory search results with word-level traceability. The company emphasizes local deployment, no cloud storage, and no model training on customer data.
Facilitate regulatory submissions for life sciences companies; Automate compliance reporting for clinical trials; Manage regulatory data across multiple jurisdictions; Streamline interactions with regulatory agencies; Enhance data accuracy in regulatory documentation
Ritivel offers an AI-native regulatory platform specifically designed for the life sciences sector. Their main product offerings include:
Clinical Study Reports (CSRs): This feature automates the drafting process, enabling users to generate CSRs in "minutes, not weeks," with word-level traceability to ensure accuracy and compliance.
CTD Automation: This tool facilitates literature searches and automatically drafts summaries for regulatory submissions, streamlining the process for regulatory affairs professionals.
Regulatory Search: Ritivel provides instant access to FDA and ICH guidelines, allowing users to find relevant regulatory information without the need for signup.
Key features and benefits of Ritivel's offerings include:
These features collectively help regulatory affairs professionals and compliance officers in the pharmaceutical industry to navigate complex regulatory challenges more efficiently.
Backed by Y Combinator W26; Serves clients in the life sciences sector; Focused on regulatory compliance challenges