Regulatory specialists are integral to bringing novel medical devices to market. They require a breadth of managerial and interpersonal skills in addition to technical, clinical and legal knowledge. The program of Advanced Studies in Medical Device Regulatory Affairs (RA) and Quality Assurance offers career specialised training for graduate students based on the newly implemented European Medical Device Regulations (MDR).
In addition, the course provides participants with comprehensive knowledge and practical experience in: international RA, quality management, risk management, clinical evaluation of medical devices, technical writing and leadership.
Participants of this program will receive a MAS/DAS accredited by the University of Bern after successful completion.
What to expect from this program?
Who is this program for?
Recent graduates will will increase their career projects in an industry that is currently in need of trained professionals. The industry-based learning placement is a unique opportunity to gain insight into the industry.
Mid-level experienced professionals will raise their proficiency to the next level, that allows them to approach different career options. The close collaboration with peers and lecturers expand your network internationally.
Study Program and Learning Environment
The program is taught in a blended learning environment, allowing for flexible education that complements part time professional work. The courses utilise e-learning, peer learning and interactive discussions with experts, on site lectures, workshops and case studies. The MAS program additionally includes an industry based learning placement in the second year of study. Class sizes are limited to ensure high quality personal education that fosters communication and professional networking.
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Freiburgstrasse 3, Bern, Switzerland