Master of Science in Pharmaceutical Regulatory Affairs

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

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.

The fees for Master of Science in Pharmaceutical Regulatory Affairs may vary from €5,000 to €15,000 annually for tuition fees. The fee's prices may get higher for International Students.