Master in
Quality, Regulatory, Clinical & Medical Affairs in Medical Devices & In Vitro Diagnostics

1st Edition

Reasons to take the course

The demand for training in the field of medical devices and in vitro diagnostics is growing all the time. This programme combines the knowledge of the essential areas for the development, production and commercialisation of biotechnological devices of medical importance. This set of skills is essential both for those who wish to work in biotechnological companies and for those who wish to develop their own designs by starting up a new company.

Presentation

The biotechnological revolution of recent decades has transformed healthcare systems around the world. One of the biggest successes of biotechnology is the development of new medical devices (MD) and in vitro diagnostic (IVD) tests, which are now fundamental for human medicine. Such diagnostic tools must fulfil an extensive set of legal requirements that are controlled by regulatory agencies, as is the case with new drugs or therapies. The requirements for MD and IVD are quite specific, but while there is high demand worldwide for experts in this field, there are very few opportunities to learn the required skills.

The Master in Quality, Regulatory, Clinical & Medical Affairs in Medical Devices & In Vitro Diagnostics aims to provide solid training in all the aspects (including quality, regulatory, clinical and medical affairs) involved in developing and commercialising any medical or in vitro diagnostic device.

Promoting entities

Collaborating entities

  • Ambit Building Solutions Together
  • Qiagen

Get the head start you need to become a professional in the Medical Devices and In Vitro Diagnostic industries

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