• Search BSI
  • Verify a Certificate
BSI Home page
Contact Us
Search Icon
Back to menu Choose a country/region

No countries/regions found

Suggested region and language based on your location

    Your current region and language

    Submit
    Science, medicine and research, women in laboratory with laptop and equipment.
    • Brochure
      Medical Devices

    IVDR Amending Regulation (EU) 2024/1860 FAQs

    Guidance incorporating IVD manufacturer feedback on Amending Regulation 2024/1860 and IVDR transitional provisions implementation.

    Read the Brochure

    Guidance on IVDR transitional provisions

    Download this Read the Q&A to find out more about:

    • IVDR transition cases & Article 110.

    • Confirmation letters.

    • QMS documentation requirements.

    • Appropriate Surveillance of legacy devices.

    Insights & Media

    Learn from global experts in healthcare standards

    Get Insights & Media
    doctor checking patient mouth
    Brochure

    Innovative solutions for Sterile Medical Devices

    Read the Brochure
    Contact Us

    Let's shape your organization's future together

    Reach out and see how we can help guide you on your path to sustainable operational success.

    Get in touch
    Get in touch