This course will extend your knowledge of the stages of product development for pharmaceuticals, medical devices and other healthcare products across both animal and human health, as well as of the regulatory requirements affecting development processes and related commercialisation strategies. Biomedical and health related sectors are given specific attention given their unique and stringent development requirements. Across a range of seminars, you will learn from industry practitioners, consultants and scientists who have hands-on expertise spanning different dimensions of product development and regulatory affairs within New Zealand and internationally.
Although structured around expert seminars, classes are essentially tutorial-based in terms of their style and form of delivery, and students are expected to be active members of the class and be open to asking questions and steering discussion. Throughout the course, the emphasis is on real-world contexts and applied case examples. You will thus gain valuable, practical insights into the challenges of product development within complex regulated environments, and how these are addressed as part of product commercialisation.