Dear Market Operators There is an important survey on the sectorial regulatory governance and innovation in the field of Medical Devices (MDR) and In Vitro Diagnostic Medical Devices (IVDR), conducted by The…
Read articleThe European Commission Health and Food Safety DG SANTE has just released two Guidance documents for both Manufacturers and Notified Bodies in the realm of Medical Devices (MDR) and In Vitro Diagnostic Medical Devices (IVDR): 𝗠𝗗𝗖𝗚 𝟮𝟬𝟮𝟯-𝟱: 𝗚𝘂𝗶𝗱𝗮𝗻𝗰𝗲…
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The NoBoCap project, recently completed the first cohort of its ambitious MDR (Medical Device Regulation) master’s Level Module 1 “Implementing Regulatory Requirements for Medical Devices” led by SGS (NB 1639) and TU Dublin.
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Ready to embark on this knowledge-packed journey?
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Exciting News from the Clusters Meet Regions Conference in Iasi, Romania!
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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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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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Email: nobocap@rohealth.ro