M.Sc (Medical Technology Regulatory Affairs)
Course Overview
The programme is offered as a two year part-time Level 9 MSc in Medical Technology Regulatory Affairs (90 credits). The programme is delivered online using a combination of distance-learning / e-learning technologies and face to face workshops for an overall blended learning approach. The program consists of 12 modules, each worth 5 ECTS. Three modules are delivered per semester. A dissertation (30ECTS) is also carried out over Year 1 and year 2. Assessment of students is through continuous assessment
The MSc programme is also available for students to undertake in a modular format. Students undertaking the modular programme can select any individual module or combination of modules in any year, up to a maximum of 3 modules per semester. Students must complete all 12 taught modules and a research project within six years, to obtain an MSc degree. Postgraduate Certificate and Diplomas are also available as exit degrees, based on the completion of 6 or 12 taught modules.
Program objectives are to:
- Produce graduates with the essential breadth and knowledge, skills and competencies required to work as a regulatory affair professional in the Medical Technologies industry sector
- Provide participants with professional skills and knowledge to conduct appropriate advanced data analysis and interpretation in a highly regulated environment
- Enable participants to effectively communicate and defend scientific data and findings in a variety of forms to regulatory agencies, medical care systems, internal personnel and the public
- Provide participants with the skills and ability to function within, and adapt to, a changing medical technologies environment with rapidly evolving regulatory frameworks
- Prepare participants to provide strategic, tactical and operational direction and support to expedite the development and delivery of safe and effective healthcare products to the required regulatory standards
Scholarships Available
Intakes
- Sep
Application Processing Time in Days: 30
Minimum English Language Requirements
English Level Description | IELTS (1.0 -9.0) | TOEFL IBT (0-120) | TOEFL CBT (0-300) | PTE (10-90) | |
---|---|---|---|---|---|
Expert | 9 | 120 | 297-300 | 86-90 | |
Very Good | 8.5 | 115-119 | 280-293 | 83-86 | |
Very Good | 8 | 110-114 | 270-280 | 79-83 | |
Good | 7.5 | 102-109 | 253-267 | 73-79 | |
Good | 7 | 94-101 | 240-253 | 65-73 | |
Competent | 6.5 | 79-93 | 213-233 | 58-65 | |
Competent | 6 | 60-78 | 170-210 | 50-58 | |
Modest | 5.5 | 46-59 | 133-210 | 43-50 | |
Modest | 5 | 35-45 | 107-133 | 36-43 | |
Limited | 4 | 32-34 | 97-103 | 30-36 | |
Extremely Limited | < 4 | < 31 | < 93 | < 30 |
Admission Requirement / Eligibility Criteria
Entry Requirements
Candidates must hold a least a Second Class Honours Level 8 primary degree in a related subject area in science or engineering and at least two years’ prior relevant experience in the medical technology industry. Prior medical technology industry experience in regulatory affairs will be considered a distinct advantage in assessing applications. Applications from candidates who hold a relevant degree at Level 7, with at least two years’ medical technology industry experience in regulatory affairs, will also be considered.
- Course Type: Part Time
- Course Level: Masters/PG Degree
- Duration: 02 Year
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Total Tuition Fee:
18000 EUR
Annual Cost of Living: 12150 EUR
Application Fee: 35 EUR
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