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so good afternoon everyone my names catherine fuller and im the assistant director of the post-market reforms and review section in the medical device surveillance branch branch of the therapeutics goods administration before i start id like to acknowledge the traditional custodians of the land on which we all meet today wherever you are situated and pay my respects to their elders past and present i extend that respect to aboriginal and torres strait islander people here with us today on this webinar thank you for joining us today to discuss the application process for consent to import supply or export medical devices that are non-compliant with the essential principles as this is a bit of a mouthful from here on in ill just refer to it as the consent to supply form the tga is modernizing this process to move from a standalone paper-based form to an online form the transition has occurred in two phases with the first phase being on interim online form hosted on the tga consultat