This programme will introduce and explore the medical device industry in Ireland and provide an understanding of the design, development, manufacturing, validation and testing process for medical device technologies and the role of the regulatory affairs officer in advising on the suitability of development programmes from a regulatory perspective.
Entry Requirements
All applicants will be considered on a case-by-case basis. Lifelong Learning reserves the right to require applicants to attend for an interview to determine their suitability for the programme
