Viewing the right FDA WL is helpful, analyzing 100K+ enforcement documents is powerful

Dive into the most complete database of FDA WLs and global enforcement documents.

This demo will teach you how to:

  • Search by agency, source, GxP, industry, inspection reason, and more
  • Locate FDA Warning Letters by date, company, FDA office, or subject
  • Learn about your investigator with comparison metrics, trends, and citation lists

    Built for experts by experts, Redica Systems’ platforms help you turn data into immediate, actionable insights

    Integrated data, intelligence,
    visualizations, and workflows


    Unmatched Data

    Proprietary data sourcing powered by the Freedom of Information Act (FOIA)
    and web crawling from >15,000 individual data sources

    • >200 Agencies and Standards bodies
    • Industry coverage includes: Human Drugs, Biologics, Medical Devices & IVD, Combination Products, Animal Health, and Food
    • GxP coverage includes: GLP, GMP, GCP, GMP for IMP, GVP, and GDP
    • >4,500 Inspector Profiles
    • >300,000 Site and Organization Profiles
    • >100k regulatory documents – 483s, Warning Letters, Untitled Letters, Certificates of Non-Conformance, Regulations, Guidance, etc

    Deep Intelligence

    We seamlessly integrate data science capabilities with expert intelligence- including AI, natural language processing, machine learning, into the data pipeline to extract additional value.

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    Bringing everything together

    Our team assimilates, normalizes, and categorizes large amounts of unstructured data to make sure all entities are represented and connected. The RedicaID provides a real-time view into evolving data by tracking inspections, enforcement actions, regulatory publications, and M&A activity. In a complex landscape that’s always in flux, the RedicaID is a reliable constant.

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