In September and October 2025, the Therapeutic Goods Administration (TGA) hosted 2 UDI sponsor workshops aimed at helping sponsors understand the Australian implementation of the UDI system and the AusUDID. The sessions built awareness, clarified requirements, identified remaining details to be solved, and strengthened engagement across the medical device sector.
Speakers
- Gary Pascoe, UDI Project Lead, Devices Reforms Taskforce, TGA
- Tracey Duffy, First Assistant Secretary, MDPQD Executive BR, TGA
- Carolyn Wilson, MDPQD Executive BR, TGA
- Anabela Firman, MDPQD Executive BR, TGA
Slides
Slides presented during the UDI Roadshows, including an overview of UDI requirements, compliance timeframes and stakeholder responsibilities.
We aim to provide documents in an accessible format. If you're having problems using this document, contact tga.education@tga.gov.au.
Questions and answers
Responses to questions asked during the UDI Roadshow.
Content in this document is correct at the time of publication. It will not be updated. Current information can always be found on the UDI Hub.
Summary
An overview of the UDI Roadshow, including.
- attendees
- feedback received
- next steps.