Registration is now open for Module 2 – Generating Data for Technical Documentation (MDR), part of the NoBoCap postgraduate training programme dedicated to strengthening regulatory capacity in the medical devices…
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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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BRINGING TOGETHER EUROPETO UNLOCK MEDICAL DEVICE REGULATIONS & THE AI ACTFOR INNOVATORS AND SMES IN EUROPE 15-16 October 2025 Brussels, Belgium Download presentations Hear the speakers discuss building your knowledge…
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Email: nobocap@rohealth.ro