South East Technological University, Ireland
Dive into the intricacies of regulatory affairs with our specialized program, offering a comprehensive perspective on the regulatory landscape. Our program goes beyond conventional boundaries, offering an in-depth exploration of current and anticipated EU legislation. Geared towards medical device regulatory affairs, this initiative equips students with advanced theoretical knowledge crucial for navigating the complex processes and practices inherent to the field. Elevate your understanding of regulatory affairs and position yourself at the forefront of compliance in the ever-evolving landscape.
Under Graduation: 60%
IELTS: 6.5
Duolingo : 110
Course Description: This program is designed to provide students with in-depth knowledge and skills in regulatory affairs specifically tailored for the medical device industry. It covers a range of topics including regulatory frameworks, quality management systems, clinical trial regulations, and the submission processes for gaining approval from regulatory authorities.
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