This is a practical half-day workshop designed for those in sales, marketing, product development, and other non-regulatory roles who need to understand Australia's medical device regulations. Through interactive case studies, real-world scenarios, and hands-on activities, participants will learn how medical devices are classified, the pathways used to bring them to market, and key compliance requirements. The workshop will also focus on effective collaboration with regulatory teams to ensure business success while meeting TGA regulations.

Join an immersive, one-day training designed to bridge the gap between theory and real-world HTA practice.