Regulatory Affairs for Medical Devices
Dublin, Ireland
Regulatory Affairs for Medical Devices at Trinity College Dublin is a comprehensive program designed to equip students with in-depth knowledge of European medical device regulations. The course addresses the recent overhaul of the EU Medical Device Regulation (MDR), exploring its implications for market dynamics and the medical device ecosystem. Delivered by industry experts and regulatory specialists, the program emphasizes practical application and strategic compliance, preparing graduates for roles in MedTech organizations with a focus on regulatory responsibilities and product lifecycle management.
- Dublin, Ireland
- 2 years
- On Campus
- ₹13,71,930/Year
Pros & Cons
Not enough reviews to generate pros and cons
Program Overview
Regulatory Affairs for Medical Devices at Trinity College Dublin is a comprehensive program designed to equip students with in-depth knowledge of European medical device regulations. The course addresses the recent overhaul of the EU Medical Device Regulation (MDR), exploring its implications for market dynamics and the medical device ecosystem. Delivered by industry experts and regulatory specialists, the program emphasizes practical application and strategic compliance, preparing graduates for roles in MedTech organizations with a focus on regulatory responsibilities and product lifecycle management.
QS World Ranking
Not Available in Not Available
Class Size
400 Students
Key Features
Specializations Available
AI/ML, Systems, Theory, Human-Computer Interaction
Research Opportunities
Access to cutting-edge research labs and industry partnerships
Admission Requirements
TOEFL®
88.0
Key Dates
Application Start time & Deadline
Starting 2025-09-01
Apply before 2025-07-01
Program Start
Sep-25, 2026-09-01 00:00:00, 2026-01-01 00:00:00
Programme Structure
Courses include: Clinical Investigations Clinical Evaluation, Post-Market Assessment Biocompatibility and Medical Devices Risk Management and Medical Devices Quality Management and Conformity Assessment Pathways Qualification, Classification, Borderline Products and Device Traceability Preparing A Clinical Development Plan for a Novel Active Implanted Medical Device Regulatory Policy Research Project And Dissertation
Program Highlights
- Comprehensive curriculum covering all key topics
- Hands-on projects and real-world case studies
- Expert faculty with industry experience
- Career support and placement assistance
Academic Requirements
GPA
3.5
English Language Requirements
TOEFL®
88.0
Overall ScoreAdditional Requirements
Applicants should possess an Honours Bachelor's degree, preferably at 2.1 level or higher, in disciplines such as pharmacy, medicine, allied health professions, biomedical engineering, biology, or law. Consideration may be given to candidates from other fields based on individual assessment, which may include an interview to evaluate suitability. While prior experience in MedTech development, manufacturing, or regulation is advantageous, relevant professional experience in related areas is also welcomed for application eligibility.
Course Fees
₹13,71,930/Year
Annual Fee
2 years
Total Duration
Living Costs
No Living costs available.
University Scholarships
No University Scholarships Available
External Scholarships
Rochelle Nicolette Perry Memorial Scholarship
N/A
Amount
1250 USD
Deadline
Not specified
Organization of American States (OAS) Academic Scholarship Program
N/A
Amount
Various benefits
Deadline
Not specified
Master's Scholarship
N/A
Amount
Various benefits
Deadline
Not specified
Denise Halbach Performance Scholarship
N/A
Amount
2000 USD
Deadline
15 Apr 2025
Thomas Jefferson Prize in United States History
N/A
Amount
300 EUR
Deadline
Anytime
Eligibility Requirements
No Eligibility Requirements Available
Application Process
No Application Steps Available
News About Abroad
No news articles found
