Save the Date: Module 3
We’re just one month away from the start of Module 3 – Generating Data for Technical Documentation (IVDR), beginning on April 14th in collaboration with SGS and Technology University Dublin!…
Read articleWe’re just one month away from the start of Module 3 – Generating Data for Technical Documentation (IVDR), beginning on April 14th in collaboration with SGS and Technology University Dublin!…
Read articleThe application process for Module 1, starting on February 10, 2025, is now officially closed. Don’t worry—your application will be considered for the next session, which is planned for Summer…
Read articleUnlock the skills you need to become an expert in Medical Devices Regulation (MDR) with our online postgraduate-level courses! Whether you’re aiming to work in medical device manufacturing, auditing, or…
Read articleThe 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…
Read articleAre you ready to take your understanding of In Vitro Diagnostic Medical Device Regulation (IVDR) to new heights?
Read articleSUMMIT 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…
Read articleOn 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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