Short Course on Training for C-level Management of MO’s on MDR/IVDR Implementation and Resource Allocation
Are you ready to navigate the complex world of EU Regulations in the Medical Device Industry?
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Post-Webinar: Building a Community for Innovators to Unlock the EU Regulations
We’re thrilled to have hosted today an insightful event for the NoBoCap Community. At the event, we dove deep into the initiatives aimed at unlocking EU regulations for innovation. Our…
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Notified Bodies Survey on Certifications and Applications (MDR/IVDR) – updated document
The latest “Notified Bodies Survey on Certifications and Applications (MDR/IVDR)” is now available!
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CORE-MD Webinar | Providing high-risk medical devices for children – problems and proposals
Ready to embark on this knowledge-packed journey?
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Clusters Meet Regions Conference, Iasi, Romania, 21-23 November 2023
Exciting News from the Clusters Meet Regions Conference in Iasi, Romania!
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Brief Online Survey for Market Operators
We Need Your Insights for shaping the training curriculum developed under the NoBoCap Project! Participate in Our Brief Online Survey! Your voice is crucial. By taking a few minutes to…
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Post-Webinar: Building a Community for Innovators to Unlock the EU Regulations
It was marked a pivotal moment in the NoBoCap initiative’s journey, as we hosted an interesting webinar dedicated to forging a dynamic community of innovators, united by a common goal:…
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Notified Bodies Survey on certifications and applications (MDR/IVDR) – updated document
The Commission’s Directorate-General for Health and Food Safety has just released an important update for those closely following Medical Devices and In Vitro Diagnostic Medical Devices Regulations (MDR and IVDR). The “𝐍𝐨𝐭𝐢𝐟𝐢𝐞𝐝 𝐁𝐨𝐝𝐢𝐞𝐬…
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FREE WEBINAR: Building a Community for Innovators to Unlock the EU MDR/IVDR Regulation
Join us in a webinar presenting the NoBoCap initiative on Building a Community for Innovators to Unlock the EU MDR/IVDR Regulation. NoBoCap is an EU co-funded project aiming to empower…
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The Latest Version of the Manual on Borderline and Classification under MDR and IVDR is Here!
The latest updates in the world of medical device regulations in Europe.
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