Events

Guidance on completing updated notification form for new therapeutic vaping products, and information on the re-statement of compliance when requested by TGA.

See the upcoming changes in the PRAC – the new procedure document that will replace the Uniform Recalls Procedure for Therapeutic Goods (URPTG).

Hear about the options we currently considering in relation to the future regulation of assistive technologies. Q and A session included.

View the proposed changes to the post-market review compliance portal allowing sponsors of exempt devices to view and respond to regulatory notices, and ask questions and provide feedback on the proposed changes.

View the proposed changes to the on-line application form for consent to import, export, or supply medical devices that do not comply with the Essential Principles.

This webinar provides information about the TGA’s public consultation paper on the proposed changes to the Australian Essential Principles and an opportunity to ask questions.

Presented at the ARCS Annual Conference 2024.

Presented at the ARCS Annual Conference 2024.

Presented at the ARCS Annual Conference 2024.

Presented at the ARCS Annual Conference 2024.

Presented at the ARCS Annual Conference 2024.

Presented at the ARCS Annual Conference 2024.

Webinar 1 Wednesday May 8. Webinar 2 Friday May 10.

This presentation is about our revised guidance on advertising health services which involve cosmetic injectables.

This webinar provides information on the TGA’s public consultation on the impacts, challenges and opportunities relating to medicine shortages.

The TGA Good Manufacturing Practice Forum returned to Sydney on 21 March 2023.

In this webinar we will provide an update on the Australian UDI implementation and discuss the challenges and benefits of having UDI in healthcare and the role of hospitals and other healthcare providers in relation to using UDI.

A webinar covering how to view and respond to notifications in the Consent for Non-compliance Dashboard

A webinar covering medical device that are non-compliant with the Essential Principles (EPs)

This webinar will guide you through the process of applying for consent to import, supply or export a medical device non-compliant with the Essential Principles (EPs)

Guest speakers from Zebra Technologies will share observations and learnings from the UK Scan4Safety pilot.

The TGA SME Assist presents 'Meeting your Obligations', a free workshop aimed at beginners who are unfamiliar with therapeutic goods regulation.

Information for manufacturers, sponsors and users of the UDI data on how to access the AusUDID Sandpit

Information for manufacturers, sponsors and users of the UDI data on how to access the AusUDID Sandpit

Information for manufacturers, sponsors and users of UDI data on how to access the AusUDID Sandpit