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 to enhance regulatory expertise and ensure compliance with the EU Medical Device Regulation (MDR 2017/745) and the In Vitro Diagnostic Regulation (IVDR 2017/746).

Available Modules:
Module 1 – Implementing Regulatory Requirements for Medical Devices
Starts: 16 September 2025
Registration deadline: 8 September 2025

Module 3 – Generating Data for Technical Documentation (IVDR)
Starts: 16 September 2025
Registration deadline: 8 September 2025

Each program runs for 10 weeks (100 hours total) and awards a 5-credit EQF7 Certificate, accredited by the University of Medicine, Pharmacy, Sciences and Technology of Târgu Mureș (Romania).

Don’t miss this final opportunity to access high-quality training, gain practical knowledge, and obtain a recognized academic certification – all free of charge.

REGISTER RIGHT NOW HERE: https://portal.nobocap.eu/