Pharmaceutical Regulatory Affairs

Institute of Technology Carlow - Carlow Campus

 

Course Name Pharmaceutical Regulatory Affairs
Course Provider Institute of Technology Carlow - Carlow Campus
Course Code CWS03 CWL11 CWS04 CWL12
Course Type Postgraduate
Qualifications
Award NameNFQ ClassificationAwarding BodyNFQ Level
Degree - Masters (Level 9 NFQ)  More info... Major QQI Level 9 NFQ
Postgraduate Diploma (Level 9 NFQ)  More info... Major QQI 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+Please note that all postgraduate applications for taught programmes at Institute of Technology Carlow should be completed online via PAC (Postgraduate Application System) www.pac.ie

Application process steps

1. Choose your programme(s) from o...

Application Weblink Web Page - Click Here
Duration 1 year full-time, 2 years part-time.
Course Fee CWS03 Master of Science in Pharmaceutical Regulatory Affairs CARLOW Full-time 9 90 €7,400*

CWL11 Master of Science in Pharmaceutical Regulatory Affairs CARLOW Part-time 9 90 €7,400*

CWS04 Postgraduate Diploma in Pharmaceutical Regulatory Affairs CARLOW Full-time 9 60 €5,500

CWL12 Postgraduate Diploma in Pharmaceutical Regulatory Affairs CARLOW Part-time 9 60 €5,500

*Fees for ITC Major Award graduates only – €5,500.
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...

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
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 of...

Further Enquiries Lifelong Learning
Joseph Collins
BA, HDipEd, STB, MEd, STL
E: LLL@itcarlow.ie