Pharmaceutical Regulatory Affairs - Carlow

SETU - Carlow Campus

 

Course Name Pharmaceutical Regulatory Affairs - Carlow
Course Provider SETU - Carlow Campus
Alternative Provider(s) SETU - South East Technological University
Course Code SE51D SE51A SE51E SE51B
Course Type Postgraduate
Qualifications
Award NameNFQ ClassificationAwarding BodyNFQ Level
Degree - Masters (Level 9 NFQ)  More info... Major South East Technological University Level 9 NFQ
Postgraduate Diploma (Level 9 NFQ)  More info... Major South East Technological University Level 9 NFQ
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Attendance Options Full time, Part time, Evening, Daytime, Weekend
Location (Districts) Carlow Town
Qualification Letters MSc/PGDip
Enrolment and Start Dates Comment Start Date: September 2023
PAC Application Information

Expand+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 F...

Application Weblink Web Page - Click Here
Duration 1 year full-time, 2 years part-time, 2 evenings per week and some Saturdays (indicative).
Course Fee 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.
Link to Course Fee Web Page - Click Here
Entry Requirements

Expand+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 sign...

Comment Exit award: Postgraduate Diploma in Science in Pharmaceutical Regulatory Affairs (Level 9 - 60 credits).
Course Summary Overview
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.
Course Content

Expand+What will I be able to do when I finish this programme?
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 ...

Subjects Taught 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
Number of Credits Master of Science in Pharmaceutical Regulatory Affairs 90 Credits

Postgraduate Diploma in Pharmaceutical Regulatory Affairs 60 Credits
Careers or Further Progression

Expand+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 emerg...

Further Enquiries Contact
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
Course Web Page Web Page - Click Here