EU MDR transition webinar #3 – consent to supply and market notifications

This is the last 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 consent to supply and market notifications, and what the Therapeutic Goods Administration (TGA) is doing to streamline the transition process.

Presenters

Dr Xin-Lin Goh, Director, Devices Applications, TGA
Merryn Steer, Acting Director, TGA
Craig Davies, TGA

Webinar details

When: Tuesday, 13 December 2022

Where: Online

Time: 1.00 - 2.00 pm AEDST

Register for webinar - external site