Course Code: REGA 5021
Academic Year: 2024-2025
This course will allow students to embark on a comprehensive exploration of health product development and regulatory affairs. Learners will explore the driving forces, steps, timelines and costs associated with discovery and development. Students will gain insights into pharmacology, toxicology, and clinical trial phases, while navigating the ethical considerations and regulatory frameworks that govern various industries. From understanding the roles of regulatory agencies to mastering process development and quality assurance, this course will equip students with the knowledge and skills needed to excel in the dynamic world of pharmaceuticals, medical devices and natural health products.