We will have limited operations from 15:00 Wednesday 24 December 2025 (AEDT) until Friday 2 January 2026. Find out how to contact us during the holiday period.
This is the second in a series of three educational webinars outlining what regulatory actions are required as a result of changes under the EU MDR, with a focus on manufacturer evidence and variations to the ARTG, and what the Therapeutic Goods Administration (TGA) is doing to streamline the transition process.
Presenters
Dr Xin-Lin Goh, Director, Devices Applications, TGA
Webinar details
When: Wednesday, 7 December 2022
Where: Online
Time: 2.00 - 3.00 pm AEDST