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MEDICA 2026

  • Location

    Dusseldorf, Germany

  • Start

    Nov 16, 2026

    10:00 AM

  • End

    Nov 19, 2026

    4:00 PM

  • Time Zone

    Belgrade, Bratislava, Budapest, Ljubljana, Prague (+01:00)

Join us at MEDICA 2026 and discover how we help medical device manufacturers navigate regulatory complexity, demonstrate compliance and bring safe, high-quality products to global markets with confidence.

With more than 4,800 exhibitors from 70 countries, MEDICA 2026 offers a unique opportunity to explore emerging technologies, gain insight into evolving requirements and stay ahead of the trends shaping the future of healthcare. This year's program highlights healthcare innovation through dedicated forums, expert-led conferences and keynote presentations spanning medicine, business, science and policy.

Visit our team to discuss how we can support your organization throughout the product lifecycle, from regulatory and market access strategies to testing, verification, cybersecurity, quality assurance and validation services. Whether you are developing connected medical devices, adopting AI-enabled technologies, manufacturing wound care products, personal protective equipment (PPE), diagnostics, implants or other healthcare solutions, or managing established product portfolios, we can help you address evolving requirements, manage risk and support efficient market access.

Learn more about our portfolio of services, including:

  • Market access – MDR, IVDR, FDA, UKCA, MDSAP and global approvals
  • Testing and verification – safety, EMC, wireless, performance, packaging, sterility, biocompatibility and chemical and microbiological testing
  • Cybersecurity and software assurance – software validation, cybersecurity assessments and support for connected and AI-enabled devices
  • Quality and compliance assurance – ISO 13485, auditing, risk management, inspections and conformity assessments
  • Validation and human factors – usability engineering, packaging validation, sterilization and reprocessing validation
  • Training – standards compliance, regulatory requirements and quality systems

As a global provider of testing, inspection, certification and regulatory support services, we help manufacturers bring medical devices and healthcare products to market safely, efficiently and in compliance with applicable requirements.

Meet our team at Booth G56, Hall 10 or at Booth D80, Hall 3, to discuss your requirements and explore practical solutions that support compliance, strengthen product confidence and accelerate market access.

For further information, please contact:

Selene Ma
Marketing Supervisor
Connectivity & Products
t:+886 (02) 2299-3939

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