We are excited to invite you to the NoBoCap Community Online Webinar, where we will come together as clusters, innovation hubs, knowledge and supportive partners to share insights and prepare for a successful year ahead. Join us to learn about our initiatives, tools, and plans. Event Details: Date: Thursday, December 19, 2024 Time: 10:00–12:00 CET…
Mark your calendars for 10-12 February 2025 and join us for an immersive 3-day training in Leuven! Here’s a glimpse into what awaits you in our upcoming modules: Module 1 – Introduction to the Course and the Regulatory Background Module 2 – Introduction to AI Module 3 – AI Evaluation and Model Performance Metrics Module 4 – Introduction…
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 product assessment, this module is your first step toward achieving MDR compliance. It’s a 10-week, 100% online course that offers 5 CPD credits and a…
We are pleased to invite you to the upcoming monthly webinar of the NoBoCap European Community of Innovation Hubs, Clusters, and Partners focused on unlocking MDR/IVDR regulation for innovation. This virtual meeting will bring together Innovation Hubs, Clusters, and Partners to collaborate on unlocking MDR & IVDR for innovation. 📅 Date: 20 February 2025 📌…
Master the Art of IVDR Compliance with Our Online Postgraduate Course! Need to navigate the complexities of the In Vitro Diagnostic Devices Regulation? This is your chance to gain the expertise needed to construct a Technical File and Performance Evaluation Report - two essential elements for regulatory compliance. Module 3: Generating Data for Technical Documentation…
MDR/IVDR Implementation and Resource Allocation for C-level Management of MOs is a specialized short course designed for C-level executives. It offers practical training on how to effectively allocate time, budget, and other essential resources needed by Market Operators to prepare comprehensive dossiers for Notified Bodies. 🔹 First step! Create your account on the NoBoCap Environment at https://portal.nobocap.eu.🔹 Then, go to…
Master MDR Compliance with Our Online Postgraduate Course! 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 – two critical pillars for regulatory compliance. Module 2: Generating Data for Technical Documentation (MDR) is a…
Summit by NoBoCap Community unlocking the MDR/IVDR regulation for innovators in Europe. The Summit will take place between 15-16 October, two days of in-person high-level dialogues and sessions, in Brussels. Hear the speakers discuss building your knowledge about MDR\IVDR requirements, gain insights from EC Representatives on the evolving EU regulatory environment, and participate in workshops and…
MDR/IVDR Implementation and Resource Allocation for C-level Management of MOs is a specialized short course designed for C-level executives. It offers practical training on how to effectively allocate time, budget, and other essential resources needed by Market Operators to prepare comprehensive dossiers for Notified Bodies. 🔹 First step! Create your account on the NoBoCap Environment at https://portal.nobocap.eu.🔹 Then, go to…
First step! Create your account on the NoBoCap Environment at https://portal.nobocap.eu. Then, go to the NoBoCap Courses section and register for The NoBoCap Short Course on Performance Evaluation of AI-based MDSW. Why This Course Matters: In a fast-evolving world of AI-driven healthcare, the ability to distinguish a well-evaluated model from a poorly assessed one is important. This hands-on course will not only teach…
Email: nobocap@rohealth.ro
