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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The certification process and increased costs slow the growth of the medical devices market
Science and technology grow rapidly, and so does the supply of medical devices. It is estimated that there are more than 500 000 types of medical devices and in vitro diagnostic medical devices on the EU market.
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Start-ups left hanging in EU medical device regulation snarl-up
Delays in getting the CE mark for medical devices are stretching the resources of European start-ups and forcing some to turn their attention to the US Europe is facing a…
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