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?
Read articleAre you ready to navigate the complex world of EU Regulations in the Medical Device Industry?
Read articleWe’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…
Read articleAre you ready to take your understanding of Medical Device Regulation (MDR) to new heights?
Read articleThe latest “Notified Bodies Survey on Certifications and Applications (MDR/IVDR)” is now available!
Read articleAre you ready to take your understanding of Medical Device Regulation (MDR) to new heights?
Read articleDear 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…
Read articleThe 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.
Read articleReady to embark on this knowledge-packed journey?
Read articleExciting News from the Clusters Meet Regions Conference in Iasi, Romania!
Read article