Notified Body designation and scope, the impact of Brexit and Competent Authority and Notified Body interpretation of the regulations. Make sure you are up to date!
Events
Training
Articles & Video
How the changing EUDAMED timeline impacts implementation of the EU MDR - with Eudamed.eu CEO Richard Houlihan
Diversity and InclusionSURVEY: Diversity, Equity and Inclusion in the Life Sciences 2021
Changes to the ISO 10993-23 and its impact on the medical device industry with NAMSA
MedTechEU Notified Body Association Takes Steps to Allay EC's Virtual Audit Fears
EU MDR & IVDRMDR and IVDR: Onsite or offsite audits? That’s the question.
Let us help you engage qualified decision makers in need of experts and services to ensure compliant medical device products. Share your strategy and plans so we can help you identify the best opportunities to reach your objectives. Our team will collaborate with you to develop a bespoke program tailored to your unique needs.
To find out more about sponsor opportunities, contact Linda Cole:
linda.cole@informa.com | +44 207 017 6631
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