In Vitro Diagnostic Medical Device Regulation (IVDR) Postgraduate Training
Are you ready to take your understanding of In Vitro Diagnostic Medical Device Regulation (IVDR) to new heights?
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SUMMIT BY NOBOCAP COMMUNITY
SUMMIT BY NOBOCAP COMMUNITY UNLOCKING THE MDR/IVDR REGULATION FOR INNOVATORS IN EUROPE September 24-25, 2024 Brussels, Belgium Go to registration Hear the speakers discuss building your knowledge about MDR/IVDR requirements,…
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Updates to MDCG 2022-4
On 27 May 2024, The Medical Device Coordination Group (MDCG) has released an update to the MDCG 2022-4 (Rev.2) guidance document.
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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 articlePost-Webinar: Building a Community for Innovators to Unlock the EU Regulations
We’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…
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Medical Device (MDR) Postgraduate Training
Are you ready to take your understanding of Medical Device Regulation (MDR) to new heights?
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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…
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