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HubMed
      • Solutions
        • Overview
        • Medea™
        • Adam™ (still under development)
      • Industries
        • Overview
        • CRO & Regulatory Consultants
        • Medical Devices Manufacturers
        • Nutraceuticals
        • Cosmetics
      • 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 

    Welcome to HubMed at CPHI Milan 2026!


    Turn EU MDR Complexity into Clinical Confidence. See how Medea™ can reduce research-intensive CER work by up to 70% — with experts in control of every decision.

    note: our limited complimentary visitor passes are now fully allocated — thank you for the great response! You can still register as a visitor on the official CPHI Milan website and book your meeting with us below.

    Book a 1-on-1 Demo / Meeting

    We'll do our best to get back to you as soon as possible.


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    Hubmed

    • Stand 8S114 | CPHI Milan (October 6–8)

    • info@hubmed.ch

    • Via Lucino 28, Breganzona Lugano (CH)

    Why RA/QA Leaders Choose Medea™

    Up to 70% less research time

    Accelerates literature search and screening across scientific databases, depending on scope and complexity.

    Audit-Ready by Design

    Supports documentation structured in line with EU MDR 2017/745 Annex XIV.

    Traceable by Default

    Every appraisal is linked to its source evidence, making Notified Body questions easier to answer.


    Discover all the features

    📍 Visiting the Start-Up Market Zone?


    Come meet the HubMed team in person:

    CPHI Milan (October 6–8)

    🏢 HubMed Booth: Stand 8S114

    📍 Zone: Start-Up Market

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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.

    CONNECT WITH US
    • Contact us
    • info@hubmed.ch

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