- Degree
- Master of Science
- Course location
- Lübeck
- Teaching language
- • English
- Languages
- The whole programme is held in English.
- Full-time / part-time
- • part-time (study alongside work)
- Mode of study
- Fully online
- Programme duration
- 4 semesters
- Beginning
- Winter semester
- Additional information on beginning, duration and mode of study
- The lectures normally start middle/end of September. At the end and the beginning of each semester, there are two days of exams.
- Application deadline
- EU applicant and non-EU applicants: 31 August for the following winter semester
- Tuition fees per semester in EUR
- 2,500 EUR
- Additional information on tuition fees
- The fee for the online course is 10,000 EUR for four semesters.
- Combined Master's degree / PhD programme
- No
- Joint degree / double degree programme
- No
- Description/content
- The degree programme focuses on providing the regulatory knowledge and tools necessary to develop and implement an optimal regulatory strategy for medical devices, including in-vitro diagnostics.
Through hands-on training following the initial professional Bachelor's degree, students gain in-depth knowledge of the medical, chemical, biological, toxicological and clinical aspects of technical documentation for medical devices.
The programme covers not only national and European regulations, but also the intricacies of key international medical device markets such as the USA, Japan, Canada and China.
A wide range of elective modules allows you to specialise in areas such as project management, entrepreneurship, or pharmaceutical law.
At the medical technology hub in Lübeck, the online Master's degree programme in "Regulatory Affairs," which was established in 2018, complements the existing range of studies in medical technology.