Module 2: Generating Data for Technical Documentation (MDR)
May 19 - July 28
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 10-week, 100-hour online course designed for professionals looking to deepen their scientific and engineering knowledge in the Medical Devices sector. Upon completion, you’ll earn a 5-credit EQF7 Certificate, giving you advanced capabilities to meet the demands of the MDR.
🔹 First step! Create your account on the NoBoCap Environment at https://portal.nobocap.eu.
🔹 Next! Go to the NoBoCap Courses section and register for Module 2 before May 9, 2025.
Save the date! Secure your spot early – places are limited. Don’t miss this opportunity to boost your expertise in MDR compliance!
Module 2 starts on May 19, 2025.
Click here: https://portal.nobocap.eu and take the next step toward advancing your MedTech career!