Pharmaceutical Regulatory Affairs
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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 managementPharmaceutical Technology Regulatory AffairsNon Clinical and Clinical Evaluation of Pharmaceutical TechnologiesMedical Technology Regulatory AffairsPrinciples of Discovery of medicines and Development PlanningResearch methods and Technical Report WritingSpecial Populations and Biologicals and Advanced TherapiesDissertation
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