AI-Powered Regulatory Intelligence for Seamless Compliance

Navigating Japan’s rigorous regulatory environment? Whether it’s PMDA consultations, evolving device classifications, or the complexities of bilingual submissions, Freya.Intelligence eases your compliance journey.

Our AI-driven platform is tailored to support life sciences companies in Japan, addressing the unique challenges of document-intensive processes, tracking frequent updates to regulations, and the need for precision in Japanese-English regulatory interpretation.

Our Core Features

Built for Japan’s Regulatory Landscape


  • Freya.Regulations

    Access our global regulations repository, enriched with PMDA, MHLW, and JPMA sources, with DocChat and AI chatbot support in every language for effortless navigation


  • Freya.Alerts

    Get personalized global updates based on your product type, classification, and therapeutic area


  • Freya.Dashboards

    Visualize compliance trends—from device classification shifts to regulatory lead times—across modular dashboards


  • Freya.RTQ

    Reply to health authority queries faster using AI-backed responses and curated Japanese case references, significantly reducing manual workload

Key Benefits

Why Japan’s Regulatory Teams Trust Freya.Intelligence

  • Access continuously updated global regulations, including 95,000+ sources across 200+ markets

  • AI-powered support for PMDA documentation with bilingual insights

  • Instant, referenceable, and expert-verified answers in Japanese and 60+ other languages

  • Timely alerts delivered to your inbox to ensure you always stay updated

  • Built-in regulatory analytics for deeper, faster decision-making

1800+ Clients and Growing…

Trusted by Global Leaders in Life Sciences

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