The certification of medical devices and in vitro diagnostic medical devices is a critical factor for ensuring patient safety and regulatory compliance in the healthcare sector. As a member of the European Union (EU), Lithuania follows EU regulations and directives but lacks its own Notified Body to certify these devices.
Read articleAre you ready to deepen your understanding of medical AI performance evaluation?
Read articleJoin us for an exclusive Short Course designed for C-level management professionals! Here’s a glimpse into what awaits you in our upcoming sessions: 8 November 2024 – Introduction session 15…
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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 UNLOCKING MDR/IVDR REGULATIONS FOR INNOVATORS IN EUROPE New Edition Coming 15-16 October 2025 Brussels, Belgium Go to presentation OF nobocap summit 2024 or join virtually Hear…
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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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Are 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…
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Are you ready to take your understanding of Medical Device Regulation (MDR) to new heights?
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