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Study at the Institute of Technology Carlow

Carlow, Ireland

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Pharmaceutical Regulatory Affairs

Master of Science at the Institute of Technology Carlow

Programme details
Degree: Master of Science (MSc)
Discipline: Pharmacy
Duration: 12 months
Study modes: full-time, part-time

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Description:

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. The programme will also enable the graduate to develop a set of transferable skills to directly meet the requirements of a broad range of future employers including information technology, written and verbal communication skills, team working, independent research skills, data analysis and critical thinking. Teaching will involve traditional lectures supported and complemented by a managed learning environment incorporating elearning, discussion boards, and moderated online debates.

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 and applied pharmaceutical sciences in drug and biologics discovery and development.

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

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 course. 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.



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