Regulatory Affairs and Quality Management

• 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 offers career specialized training in Regulatory Affairs, Quality Management and Advanced Regulatory Affairs with particular focus on the European Medical Device Regulations. It addresses graduates interested in commencing a career in the regulation or quality control of medical devices and also targets those from complementary disciplines such as entrepreneurship, research and development, and management, seeking comprehensive and practical knowledge in this field.
• The modular structure of the continuing education program in Regulatory Affairs and Quality Mangement allows you to pursue your goals tailored to your own needs. You can start with a Certificate of Advanced Studies (CAS) in Regulatory Affairs, Quality Management or Advanced Regulatory Affairs and gradually build it up to a Master of Advanced Studies in Regulatory Affairs and Quality Management.

• Bachelor's degree from a university or university of applied sciences in the fields of natural sciences, engineering, medicine, pharmacy or law.

For further information on admission requirements, please refer to the institution's website.

CHF 31'500.-