Pharmaceutical Regulatory Affairs - Carlow
The programme enables existing regulatory affairs personnel in the pharmaceutical regulatory industry to understand all current diagnostic and medical device regulations and develop the necessary skills to work successfully in the dynamic world of regulatory affairs.
| Award Name | Postgraduate Diploma (Level 9 NFQ) |
|---|---|
| NFQ Classification | Major |
| Awarding Body | South East Technological University |
| NFQ Level | Level 9 NFQ |
| Award Name | Degree - Masters (Level 9 NFQ) |
| NFQ Classification | Major |
| Awarding Body | South East Technological University |
| NFQ Level | Level 9 NFQ |
| Award Name | NFQ Classification | Awarding Body | NFQ Level |
|---|---|---|---|
| Postgraduate Diploma (Level 9 NFQ) | Major | South East Technological University | Level 9 NFQ |
| Degree - Masters (Level 9 NFQ) | Major | South East Technological University | Level 9 NFQ |
Duration
1 Year Full-time/2 Years Part-time
Entry Requirements
A second-class honours degree in science, engineering, quality, pharmaceutical or regulatory affairs or cognate areas. Those failing to meet the classification requirement may be eligible for entry to the Postgraduate Diploma.
Candidates with significant experience in: pharmaceutical operations, quality engineering, device design, mid to senior management in industry, other professionals who wish to upskill in the regulatory affairs environment, regulatory affairs personnel themselves who want to upskill (as determined by the Institute’s recognition of prior learning policy), in addition to an honours primary degree in another discipline area may also be considered for entry.
Careers / Further progression
Study & Career Opportunities
Opportunities for graduates from this programme include progression to Level 10 (PhD) programmes in related fields of study.
According to a report from the Forfás Expert Group on Future Skills Needs, Ireland is emerging as a leading location for biopharmaceuticals with a mix of start-ups, high growth SMEs and large multinationals located here.
Industry leaders including Pfizer, Eli Lilly, Sanofi, MSD (biologics based in Carlow) and Alkermes plc. have significant investment in Ireland which has facilitated rapid growth and development of the industry.
These coupled with a strong generics industry (Wockhardt, Clonmel Healthcare both based in the South-East) provide prospective employment opportunities for graduates and key engagement partners for the programme.
More than 85 pharmaceutical companies (including nine of the top 10) operate over 100 facilities in Ireland. The industry exports around $85 billion worth of products each year and is now one of the largest exporters of pharmaceuticals in the world. This programme is designed to meet the growing demand for scientists to service the current and emerging biotechnology-based industries in Ireland in particular, the South-East, Mid-East and Midlands.
Further information
SE51D Master of Science in Pharmaceutical Regulatory Affairs CARLOW Full-time €7,400*
SE51A Master of Science in Pharmaceutical Regulatory Affairs CARLOW Part-time €7,400
SE51E Postgraduate Diploma in Pharmaceutical Regulatory Affairs CARLOW Full-time €5,500*
SE51B Postgraduate Diploma in Pharmaceutical Regulatory Affairs CARLOW Part-time €5,500
* SUSI funding not available.
Course Codes:
SE51D Master of Science in Pharmaceutical Regulatory Affairs CARLOW Full-time
SE51A Master of Science in Pharmaceutical Regulatory Affairs CARLOW Part-time
SE51E Postgraduate Diploma in Pharmaceutical Regulatory Affairs CARLOW Full-time
SE51B Postgraduate Diploma in Pharmaceutical Regulatory Affairs CARLOW Part-time
Special Features of this programme
The primary objective of this Masters is to enable learners to expand their job responsibilities and opportunities in new areas after completing the programme. It will also enable learners to create an excellent network within the pharmaceutical industry, both by meeting other regulatory professionals during the course and by interacting with industry experts while completing their dissertation research.
What subjects will I study?
Lifecycle Management, Vigilance, Surveillance and Risk management
Pharmaceutical Technology Regulatory Affairs
Non Clinical and Clinical Evaluation of Pharmaceutical Technologies
Principles of Discovery of Medicines and Development Planning
Research Methods and Technical Report Writing
Special Populations and Biologicals and Advanced Therapies
Dissertation
Exit award: Postgraduate Diploma in Science in Pharmaceutical Regulatory Affairs (Level 9 - 60 credits).
On completion of this programme, students should be able to:
- Devise and implement global strategies for drug, biologic, and device development and evaluation;
- Apply principles of basic and applied pharmaceutical sciences in drug and biologics discovery and development.
Eoin O'Brien
BA, DBS, CBS, Cert Mgmt, MBA
Lifelong Learning Manager
E: eoin.obrien@setu.ie
International (Non-EU) applicants may contact:
E: international.CW@setu.ie
P: 00353-59-9175205