Regulatory Affairs 07. May 2024 – online

Over the past decade, the healthcare, pharmaceutical and medical device industries have undergone significant changes, driven by innovations such as personalised medicine, advanced therapy products, AI and − particularly in the medical device industry − the Medical Device Regulation (MDR) and In Vitro Diagnostic Medical Device Regulation (IVDR). These regulations
not only impose stricter requirements on medical devices and software, but also require medical device manufacturers to have at least one person for regulatory compliance in their company. This highlights the growing importance of regulatory expertise in these industries.

The programmes of the MAS Regulatory Affairs equip you with the skills to navigate this highly regulated and dynamic environment. Find out more about the CAS Regulatory Affairs in Life Sciences, Regulatory Affairs Pharma and Digital Transformation in Life Sciences and other degree programmes.