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HubMed
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HubMed
      • Solutions
        • Overview
        • Medea™
        • Adam™
      • Industries
        • Overview
        • Nutraceuticals
        • Cosmetics
        • Medical Devices
        • Contract Research Organization
      • Why Hubmed™
        • Overview
        • Swiss made quality
        • Data security
        • AI-Assisted
        • PICO Framework
        • End-to-End Integration
      • Resources
        • Blog
        • Press Room
        • Medea™ | Early Adopter Program
        • Medea™ | Referral Program
        • Medea™ | CER Maintenance Calculator
        • Medea™ | ROI & Savings
      • About Us
    • Contact Us 

    Swiss Precision. AI-Assisted Innovation. Trusted Evidence.


    In the high-stakes world of Life Sciences, "good enough" is a regulatory risk. HubMed is the premier Swiss-made AI platform engineered to transform R&D for those who cannot afford to fail. We combine the rigor of Swiss engineering with cutting-edge machine-reading to ensure your research is both innovative and audit-proof.


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    Why Industry Leaders Trust HubMed

    We don’t just provide tools; we provide a unified ecosystem designed for precision and trust. Our identity is built on three non-negotiable pillars that solve the "fragmentation gap" in modern R&D.


    Swiss-Made Reliability

    Engineered with the highest standards of Swiss precision to safeguard your sensitive R&D data.


    Audit-Proof Data Continuity

    The only platform that ensures data continuity from the first preclinical molecule screening to the final clinical evaluation report—eliminating the risks of manual "Excel and Word" transitions


    AI-Assisted Evidence

    HubMed acts as an intelligent research assistant, distilling complex data so your experts can focus on high-value scientific decision-making rather than "reading fatigue."

    Solving "Reading Fatigue" with Machine-Reading AI

    Traditional R&D is bottlenecked by the overwhelming volume of scientific literature. HubMed’s engine doesn't just search; it machine-reads thousands of publications to distill actionable, evidence-based insights.

    PICO-Structured Rigor

    We utilize the PICO framework to ensure every insight is structured, traceable, and ready for Notified Body audits.

    Unmatched Scientific Depth

    Our AI-assisted engine searches PubMed and specialised databases to help your experts identify evidence gaps before they lead to regulatory findings.

    Your IP, Protected by Swiss Standards

    Security is our cornerstone. In an era of increasing digital threats, HubMed provides a "secure vault" environment for your most sensitive bioactive compounds and clinical data.

    Maximum Data Privacy

    Fully GDPR compliant and aligned with the highest Swiss data privacy standards.

    Secure R&D Data Management

    Your research remains yours. We provide a protected environment that safeguards your competitive advantage and technical documentation.


    Frequently asked questions

    Here are some common questions about why Hubmed.

    HubMed is engineered and hosted in Switzerland, adhering to the national tradition of precision, reliability, and neutrality. This ensures your software is as robust as the regulatory environments you navigate.

    By reducing literature monitoring time by 70% and eliminating the risk of failed audits (which can cost €500K–€2M per month in lost revenue), HubMed provides a clear, high-speed ROI.

    Yes. HubMed is designed to maintain Audit-Proof Data Continuity through the mandatory EUDAMED rollout and legacy device transition periods, ensuring your data remains compliant and accessible.

     Experience the Precision of Swiss AI 

    Join the future of ingredient innovation and regulatory excellence.

     

    Request a demo    Talk to a Sales Expert

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    ABOUT US

    HubMed™ is a Swiss-made, AI-assisted platform for Life Sciences R&D and regulatory compliance, connecting preclinical discovery (Adam™) with clinical evaluation under EU MDR (Medea™). 

    It accelerates research-intensive work — literature search, screening, appraisal and structured drafting — while qualified experts stay in control of every scientific and regulatory decision.

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