Medical Technology Regulatory Affairs

Located in Ireland, Atlantic Technological University is a dynamic college that offers many advantages for international students. You will find a supportive community, excellent applied learning, and teaching environments that reflect the real needs of businesses and professions in the region. With a strong focus on innovation, ATU provides opportunities for you to make significant contributions to society.

ATU offers 179 programs, covering many subjects, including engineering, business, and medicine. Specifically, the college focuses on applied learning and research environments that cater to the needs of local industries. You can expect to learn from experienced faculty and engage with different departments, all while improving your English language skills.

In Ireland, you will experience a unique cultural setting with many activities to enjoy. You will be part of a community of 19,000 students, including 4,000 international students, creating a diverse and inclusive environment. The campus provides modern facilities, and the surrounding city offers many benefits, from historic landmarks to modern amenities, making it an ideal location for you to thrive and succeed.

The Medical Technology Regulatory Affairs program is a 1-year non-degree course at Atlantic Technological University. It's for students who want to work in the medical device sector, especially with the new European Medical Device Regulation and In Vitro Diagnostic Device Regulation. The program helps students understand the global regulatory framework.

The curriculum includes modules on regulatory affairs, quality management, and medical technology regulations for the US and EU markets. Students learn about design controls, risk management, and clinical studies for the medical technology industry. They also study medical device safety monitoring and incident reporting.

Graduates can work as Regulatory Affairs Specialists, Quality Managers, or Clinical Research Associates. They can also work as Medical Device Consultants or Regulatory Compliance Specialists in the medical device industry, pharmaceutical companies, or government agencies.