NoBoCap e-seminar will provide insights into the tools NoBoCap offers in support of building out regulatory expertise and enhancing the preparedness and accessibility to the specific Notified Bodies. Agenda: 9:00 to 9:10 - WELCOME 9:10 to 9:20 - NoBoCap VOICE - ACCESSIBILITY CHALLENGES AND EU REGULATION (SME – INNOVATION) 9:20 to 9:50 - NoBoCap TOOLS…
Summit by NoBoCap Community unlocking the MDR/IVDR regulation for innovators in Europe. The Summit will take place on the 24th and 25th of September 2024, 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…
BeHEALTH brings together companies, organizations, universities, and public entities, creating the ideal environment for international partnerships, and ultimately enhancing economic competitiveness in the healthcare sector. This year, the ROHEALTH Cluster is organizing the 7th edition of the BeHealth event in collaboration with Babeș-Bolyai University of Cluj-Napoca, the Center Region Support Association, the Transilvania IT Cluster,…
Join 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 November 2024 – Required investments 22 November 2024 – NB Selection 2 December 2024 – QMS & TD Development 4 December 2024 – NPV 13…
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…
Email: nobocap@rohealth.ro
