Certificate in Medical Technology Regulatory Affairs and Quality

University of Galway (formerly National University of Ireland Galway) was established in 1845 and has grown into a leading public research university on the west coast of Ireland. With around 18,065 students and approximately 4,000 international students, the university offers a wide portfolio across five colleges including Arts, Business and Law, Engineering, Medicine and Science. Known for research strengths in biomedicine, environmental science and information technology, Galway combines strong teaching with vibrant scholarly activity.

The campus sits on the River Corrib within walking distance of Galway city centre, providing students with a lively cultural scene and easy access to the region’s natural attractions. Research institutes and international partnerships support collaborative projects and postgraduate opportunities, while teaching emphasises applied learning, professional accreditation where relevant, and student engagement. The university’s community links and industry connections help translate academic work into regional and global impact.

International students benefit from comprehensive support services, clubs and vibrant city life, plus opportunities for internships, work placements and research assistantships. A broad mix of programmes and a focus on employability equip graduates for careers or further study, and the university’s reputation for research-led teaching makes it a strong choice for students seeking a supportive campus with rich academic and cultural experiences on Ireland’s west coast.

The Certificate in Medical Technology Regulatory Affairs and Quality at University of Galway is a 1-year non-degree program providing an introduction to the product development lifecycle and the role of a Medical Technology Regulatory Affairs and/or Quality professional.

The curriculum covers regulations and skills, including Introduction to Quality Management Systems, Fundamentals of EU Medical Device Regulations, and Validation and Calibration, linking existing regulations to regulatory requirements and execution across the medical device lifecycle.

Graduates can pursue careers as Regulatory Affairs Specialists, Quality Assurance Specialists, Vigilance Specialists, R&D Engineers, or Compliance Specialists, working in medical technology companies and applying their knowledge of regulatory and quality requirements.