Medical Technology Regulatory Affairs

This part-time course provides graduate professionals working in healthcare regulatory affairs or related areas, who have already gained first-hand practical experience of handling regulatory issues, with the opportunity to obtain a formal qualification. You will gain an advanced theoretical understanding of the processes and practices central to medical device regulatory affairs.

This formal qualification is the ideal way to demonstrate your existing skills to employers and peers, and to enhance your career in regulatory affairs by developing increasing levels of competence and professionalism, a broad view of the regulatory affairs role and provides a detailed insight into current and proposed EU legislation. It offers flexibility and support for those who wish to train whilst remaining in employment and is the gold standard in the field. Delegates gain invaluable access to industry professionals and networking events to help develop their careers. It will also help you develop a set of transferable skills that will directly meet the requirements of your current or future employer including information technology, written and verbal communications skills, team working, independent research skills, data analysis and critical thinking.

Employers will benefit through the development of personnel to an increased level of competence and professionalism whilst those involved in recruiting will find it easier to identify proficiency using this gold standard.

• Kamal Sehdev
• Joan Houghton

Students benefit from a programme of visiting lecturers from industry.