Medical Devices Regulation in Practice

Delft University of Technology (TU Delft) is the Netherlands' leading technical university, founded in 1842 and located in the historic city of Delft. Renowned for engineering, technology and applied sciences, TU Delft combines rigorous academics with a strong culture of innovation. With 145 degree programs across bachelor’s, master’s and doctoral levels, the university attracts ambitious students worldwide seeking hands-on, research-led training and modern laboratory facilities.

The university is especially strong in sustainable energy, water management, urban planning and mobility, and is an active member of European research networks such as CESAER and the IDEA League. Interdisciplinary laboratories, maker spaces and industry partnerships give students access to real projects, from prototype development to city-scale simulations. Many programs are offered in English and include international exchange, internships and entrepreneurship support to help translate research into practice.

Student life in Delft blends historic town life with a vibrant campus community: student associations, design teams and start-up incubators help convert classroom ideas into careers. Career services maintain close ties with European employers, supporting internships and graduate recruitment across sectors. Prospective international students should prepare a strong academic record, a concise portfolio for design or engineering programs where required, and check scholarship and visa guidance early to make the most of TU Delft’s practical, globally connected education.

The Medical Devices Regulation in Practice program is a non-degree course for students who want to learn about medical device regulations. It's taught in English and lasts for one week. You'll learn from experts at Delft University of Technology in the Netherlands.

This program covers key topics in medical device regulation, including safety and quality standards. You'll develop skills in analyzing regulatory requirements and understanding how to apply them in practice. The course includes hands-on activities to help you learn.

After completing this program, you can pursue jobs like Regulatory Affairs Specialist, Medical Device Consultant, or Quality Assurance Engineer. You can work in the medical device industry, healthcare, or government agencies. Employers may include pharmaceutical companies, hospitals, or regulatory bodies.