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 sector.
This 10-week, 100% online course focuses on the generation of data required for MDR-compliant technical documentation, supporting professionals involved in regulatory affairs, auditing, clinical evaluation, and medical device manufacturing.
The module is particularly relevant for:
- regulatory affairs professionals
- medical device manufacturers
- notified body professionals
- SMEs looking to strengthen their teams’ MDR expertise
Participants who successfully complete the module will receive 5 CPD credits and a postgraduate certificate accredited by the University of Medicine, Pharmacy, Science and Technology “G.E. Palade” of Târgu Mureș.
Course start date: 5 May 2026
How to register
To register for Module 2:
- Create an account on the NoBoCap Portal:
www.portal.nobocap.eu - Navigate to the NoBoCap Courses section and select
Module 2 – Generating Data for Technical Documentation (MDR).
Places are limited, and early registration is recommended.
