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HubMed New
      • 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™ | Partner Program
        • Medea™ | CER Maintenance Calculator
        • Medea™ | ROI & Savings
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    Blogs
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    • AI in Life Sciences
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    1 Article
    Medical Devices ×
    EU MDR 2017/745: The Compliance Deadline That Cannot Be Ignored — And What Happens If You Miss It
    Five years after its full application, EU MDR 2017/745 is no longer a transition challenge. It is the new standard. And Notified Bodies are running out of patience. When the EU Medical Device Regulati...
    CER Clinical Evaluation Report Compliance Risk Management EUDAMED MDR (Medical Device Regulation) MDR Compliance Medical Devices Time-to-Market
    4 Jul 2026
    0 176
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    Meet HubMed at CPHI Milan 2026


    Join us in Milan (October 6–8, Stand 8S114) to see how AI-assisted, expert-controlled evidence appraisal keeps your documentation traceable and audit-ready.

    • Live Medea™ Demo: see our platform in action at Stand 8S114 (Start-Up Market Zone).

    • Featured Panel: join Acting CEO Amedeo Chiappini on Oct 8th for "Nutraceuticals: Scaling Without Breaking Supply".


    Book 1-on-1 Demo

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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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