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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Medical Device (MDR) Postgraduate Training – Module 2
Are you ready to take your understanding of Medical Device Regulation (MDR) to new heights?
Read articleSurvey: Regulatory governance and innovation in the field of medical devices and in vitro diagnostic medical devices
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 articleGuidance – MDCG endorsed documents
The 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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NoBoCap MDR Masters Level Module and Post-Program Evaluation
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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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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