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.

 

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 programme. 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.