MSc Sports Performance Analysis
The MSc Sports Performance Analysis program at South East Technological University is t...
MSc in Medical Device Regulatory Affairs
Carlow
INTAKE: September
Program Overview
The MSc in Medical Device Regulatory Affairs at SETU is a program meticulously crafted to prepare students for pivotal roles in the medical device industry. This program equips students with the knowledge and skills necessary to navigate complex regulatory requirements and ensure the safety and effectiveness of medical devices.
Curriculum: The program's curriculum is thoughtfully designed to provide students with a comprehensive understanding of medical device regulatory affairs. Courses encompass a wide range of topics, including regulatory frameworks, quality assurance, clinical evaluations, and compliance. Students gain hands-on experience with industry-standard tools and regulations, ensuring they are well-prepared to address real-world challenges in the medical device regulatory field.
Research Focus: SETU places a strong emphasis on research within the field of medical device regulatory affairs. Students are encouraged to engage in research projects that explore emerging regulatory trends, clinical trial methodologies, and the impact of international regulations on the medical device industry. The faculty, composed of experienced researchers, actively support and mentor students in their research endeavors, fostering a culture of inquiry and innovation.
Industry Engagement: One of SETU's strengths is its extensive industry connections. The MSc program incorporates practical experiences, internships, and collaborations with medical device companies and regulatory bodies, ensuring that students gain real-world exposure to the dynamic landscape of medical device regulation. This practical engagement equips graduates with the skills and knowledge needed to excel in regulatory affairs roles.
Global Perspective: SETU promotes a global perspective within its programs, including the MSc in Medical Device Regulatory Affairs. The curriculum explores international regulatory practices, global standards for medical devices, and the significance of global harmonization in regulatory affairs. The diverse student body and faculty enrich the program with a multitude of global perspectives and insights, preparing graduates for regulatory roles in a globalized medical device industry.
Location
Carlow
Score
IELTS 6.5
Tuition Fee
€ 11250
Postgraduate Entry Requirements
Academic Qualifications: A minimum of 60% or above in your previous academic qualifications is required for most postgraduate programs.
English Language Proficiency:
- IELTS: Overall score of 6.5 or 7.0, with a minimum of 6 in each section.
- TOEFL: An overall score of 90, with no less than 18 in each section.
- PTE: An overall score of 64, with a minimum of 58 in each section.
- DET (Duolingo English Test): An overall score of 100.
Students must provide:
- academic marksheets & transcripts
- letters of recommendation
- a personal statement - SOP
- passport
- other supporting documents as required by the university.
Work experience: Some postgraduate courses may require relevant work experience in the field.
It's important to note that entry requirements can vary by program and may change over time. Additionally, some programs may have additional requirements, such as interviews, portfolios, or work experience.
South East Technological University offers a range of scholarships tailored to support and recognize the academic achievements of international students. These scholarships aim to facilitate access to high-quality education and contribute to the university's diverse and dynamic learning environment.
International Merit Scholarships: These scholarships are designed to reward outstanding academic performance. They are available for both undergraduate and postgraduate students and can significantly offset tuition costs.
Research Scholarships: South East Technological University encourages international students to engage in groundbreaking research. Research scholarships may be available to assist students in various research projects, contributing to advancements in their respective fields.
Diversity Scholarships: The university recognizes the value of a diverse and inclusive student body. Diversity scholarships aim to support students from a range of backgrounds and promote multiculturalism within the university community.
Excellence in Sports Scholarships: For international students with exceptional sporting talents, excellence in sports scholarships may be an option. These scholarships recognize and support student-athletes in their pursuit of academic and athletic success.
Exchange Program Scholarships: South East Technological University encourages international exchange programs to promote cross-cultural understanding. Scholarships may be available for students participating in exchange programs with partner institutions.
Industry-Specific Scholarships: Some scholarships are designed for students pursuing specific fields of study, such as STEM (Science, Technology, Engineering, and Mathematics) disciplines, arts, or business. These scholarships may be provided in collaboration with industry partners.
Community Engagement Scholarships: The university values community involvement and engagement. Scholarships may be awarded to students who actively contribute to the local community through volunteer work and civic participation.
Graduates of the MSc in Medical Device Regulatory Affairs program at SETU have a wide array of career options available in the field of medical device regulatory affairs.
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Regulatory Affairs Specialist: Graduates can assume roles as regulatory affairs specialists, responsible for navigating regulatory requirements and ensuring compliance with laws and standards.
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Quality Assurance Manager: Opportunities exist for graduates to become quality assurance managers, overseeing quality control and assurance processes in the medical device industry.
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Clinical Affairs Manager: Graduates may work as clinical affairs managers, coordinating clinical trials and evaluations of medical devices.
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Compliance Officer: Graduates can become compliance officers, ensuring that medical device companies adhere to regulatory requirements and standards.
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Regulatory Consultant: Graduates can specialize in regulatory consulting, providing expertise to medical device companies seeking regulatory guidance and support.
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Global Regulatory Affairs Manager: Opportunities are available for graduates to work in global regulatory affairs, ensuring that medical devices meet international standards and regulations.
