The Skilled Post Graduate (Medical Device Regulatory Affairs) NanoDegree Program presents students with the opportunity to skills to employers and peers, and to enhance your career in regulatory affairs by developing increasing levels of competence and professionalism. It is the ‘gold standard’ in the field.
Students will gain invaluable access obtain a formal qualification in the medical device regulation industry. The program 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.
The medical device sector is highly diverse. It covers thousands of products – from simple bandages and spectacles, through implantable devices, equipment for screening, to the most sophisticated diagnostic imaging and minimally invasive surgical equipment. Strong growth prospects for the industry globally are driven by ageing populations, increase in chronic ailments and increasing consumer wealth driving demand in emerging economies.
Trusted by 2397 Medical Students
The Skilled Post Graduate (Medical Device Regulatory Affairs) NanoDegree Program is designed to provide the knowledge and skills needed for the development of medical devices and diagnostic techniques, including aspects of medical product regulation and of product development.
