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Amanda Craig, Director of the Devices Post-Market Reforms and Review Section at the Therapeutic Goods Administration (TGA), welcomes attendees and acknowledges the traditional custodians of the land. The webinar focuses on the application process for obtaining consent to import, supply, and export medical devices that are non-compliant with essential principles, referred to as the consent supply form. The TGA is modernizing this process by transitioning from a standalone paper-based form to an online form integrated with TGA's electronic business systems account, known as TBS eBiz. The goal is to streamline the consent application process for medical devices.