Medical Devices - Regulatory Affairs
Info evening for Medical Devices - Regulatory Affairs on 1 December at 6.00pm
On Monday 1 December at 6.00pm, we are holding an online information event about our Internal link opens in the same window:“Medical Devices - Regulatory Affairs” study programme.
The evening offers an opportunity to get to know the lecturers and those responsible for the programme. Participation is possible without prior registration. The event will take place via the online conference tool Zoom.
Regulatory requirements are of central importance for companies in the medical technology industry. With its part-time continuing education programme in Medical Devices - Regulatory Affairs (MRA), Furtwangen University offers a high-quality, practice-oriented qualification for employees in the industry.
The programme is modular and can be completed in four independent modules, each lasting four months. Alternatively, it is possible to combine all modules to obtain a master's degree from HFU. Each semester, there are four attendance phases at the Tuttlingen campus, supplemented by a blended learning concept that enables flexible learning.
In the 2025/26 winter semester, a new group successfully began the module “Medical Technology: Quality Management and Clinical Validation.” At the same time, an advanced cohort is deepening its knowledge in the field of regulatory affairs using practical case studies.
The summer semester of 2026 offers another ideal opportunity to join the programme with the module “Medical Technology: Fundamentals of Regulatory Affairs and Development Management.” The application phase for this module has already begun.
External link opens in a new window:This way to the Zoom room