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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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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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 updates in the world of medical device regulations in Europe.
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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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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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