Medical Device Regulatory Affairs

This programme presents a broad view of the regulatory affairs role and provides a detailed insight into current and proposed EU legislation. It provides students with an advanced theoretical understanding of the processes and practices central to medical device regulatory affairs. What will I be able to do when I finish this programme? This MSc will allow students to develop a set of transferable skills that will directly meet the requirements of future employers including information technology, written and verbal communication skills, team working, independent research skills, data analysis and critical thinking. What subjects will I study? Regulatory Affairs Quality Management and Strategy Research Methods and Technical Report Writing Medical Device Technologies: Design, Development and Testing Medical Technology Regulatory Affairs Product Programme Management, Vigilance, Surveillance and Risk Management Clinical Evaluation of Medical Device Technologies Research Dissertation