https://informaconnect.com/eu-ivdr-preparation-implementation-medtech-ebook/
EU IVDR Preparation and Implementation: Discover Industry, Notified Body and Competent Authority perspectives in this MedTech Summit eBook.
eu ivdrebook seriespreparationimplementationmedtech
https://www.nerac.com/services/medical-device-regulatory/
Dec 4, 2025 - Navigating medical device regulations requires a partner with comprehensive expertise, not just in compliance but in supporting the entire lifecycle of your
medical device regulatoryeu mdrneracservicesexpert
https://www.bsigroup.com/en-CZ/insights-and-media/media/webinars/renewal-under-uk-and-eu-legislations-for-mdr-ivdr-and-ukca/
Providing an overview of the process for renewals within BSI and how manufacturers should be submitting for this and what documentation is required.
renewalukeulegislationsmdr
https://www.bsigroup.com/nl-NL/insights-and-media/media/webinars/understanding-and-meeting-the-eu-ivdr-requirements-for-in-vitro-diagnostics-ivd-kits/
In vitro diagnostic medical devices (EU) 2017/746 definitions that reflect changes in technology, progress in diagnostics and regulatory oversight.
eu ivdrunderstandingmeetingrequirementskits
https://www.nsmedicaldevices.com/news/guardant-health-gets-eu-ivdr-certification-for-guardant360-cdx/
May 23, 2024 - Guardant Health has received European Union (EU) In Vitro Diagnostic Regulation (IVDR 2017/746) for its Guardant360 CDx liquid biopsy test.
guardant healtheu ivdrgetscertificationcdx
https://www.bsigroup.com/en-GB/insights-and-media/media-centre/press-releases/2024/september/rollout-of-eu-reference-laboratories-for-ivdr-class-d-devices/
Class D IVD manufacturers will gain more insights in the newly enrolled EURL regulation and will be better prepared for the engagement between BSI and the...
reference laboratoriesrollouteuivdrclass