Aims

 

  • To present a foundation of integrated knowledge in science-based medicinal product development and regulation.
  • To enable application of innovative methods, tools and strategies that best utilize recent scientific advances and technologies to medical product design, development and regulatory review.
  • To address real world challenges encountered during the development, manufacture, review and commercialization of a medical product.
  • To cover the entire medical product life cycle – from molecule to marketplace.
  • To train the leaders and integrators for medical product development.
  • To understand future directions in global pharmaceutical and health economics and business environments, and implications for product development and evaluation.
  • To provide university, regulatory and industry professionals with a platform and network for the discussion of central issues concerning drug development and new therapies.

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