Veri Kalitesi: 100/100 Kaynak: expatrio (son güncelleme 6 ay önce)

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📋 Program Hakkında

This programme deals with the approval of medical technology products, process and quality management and development processes in the field of medical devices. The master's can be completed in five semesters while working. It consists of four modules: 'Fundamentals of Regulatory Affairs and Development Management', 'Quality management and clinical validation', 'Consolidation of Regulatory Affairs', and 'Application Regulatory Affairs'. The program covers the entire product life cycle from development management to production, technical documentation, clinical evaluation and post-market surveillance, as well as areas such as materials, sterility and data analysis.

✅ Giriş / Kabul Koşulları

* Completed first degree with at least 210 ECTS credits (bachelor's, magister, diplom) * If first degree has less than 210 ECTS, additional courses or practical achievements can be recognized * First degree must be in technical engineering, natural sciences related to medicine, medicine, biology, biochemistry, business administration or law (other degrees possible if clearly related) * At least one year of relevant professional experience after completing first degree * German language skills required

Hochschule Furtwangen

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