Pharmaceutical Regulatory Affairs

SETU - Carlow Campus

 

Course Name Pharmaceutical Regulatory Affairs
Course Provider SETU - Carlow Campus
Alternative Provider(s) SETU - South East Technological University
Course Code CWS03 CWL11 CWS04 CWL12
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
Apply To PAC
Attendance Options Full time, Part time, Evening, Daytime
Location (Districts) Carlow Town
Qualification Letters MSc
PAC Application Information

Expand+Course Codes:
CWS03 Master of Science in Pharmaceutical Regulatory Affairs CARLOW Full-time

CWL11 Master of Science in Pharmaceutical Regulatory Affairs CARLOW Part-time

CWS04 Postgraduate Diploma in Pharmaceutical Regulatory Affairs CARLOW F...

Application Weblink Web Page - Click Here
Duration 1 year full-time, 2 years part-time.
Course Fee

Expand+CWS03 Master of Science in Pharmaceutical Regulatory Affairs CARLOW Full-time €7,400**

CWL11 Master of Science in Pharmaceutical Regulatory Affairs CARLOW Part-time €7,400*

CWS04 Postgraduate Diploma in Pharmaceutical Regulatory Affairs C...

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 sig...

Comment NOTE: All programmes are offered subject to sufficient numbers of students. This document is intended as a guide to programmes. While every effort has been made to ensure the completeness and accuracy of the information contained in this publication at the time of print, Institute of Technology Carlow reserves the right to make changes to any content, schedules or fees.
Course Content

Expand+What is the programme about?
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 successf...

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+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 ...

Further Enquiries LIFELONG LEARNING MANAGER
Eoin O’Brien BA, DBS, CBS, Cert Mgmt, MBA
E: eoin.obrien@itcarlow.ie
Course Web Page Web Page - Click Here
International Students Web Page - Click Here