The NoBoCap project invites professionals across the MedTech sector to register for its final training modules in 2025. These expert-led programs are offered free of charge, providing a unique opportunity…
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Need to navigate the complexities of the Medical Device Regulation (EU 2017/745)? This is your chance to gain the expertise needed to construct a Technical File and Clinical Evaluation Report…
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📣 The 3rd Edition of the C-Level Training Short Course Starts this May!
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Are you ready to strengthen your expertise in Technical File construction and Performance Evaluation Report development under IVDR (EU 2017/746)? Module 3 – Generating Data for Technical Documentation (IVDR) begins…
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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!…
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The 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…
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Unlock 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…
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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.
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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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Email: nobocap@rohealth.ro