Events

An overview of the amended sponsor portal to include unapproved medical devices and provides guidance on how to apply for consent to import, supply or export medical devices that do not comply with the Essential Principles (EPs).

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

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.

Webinar Tuesday 20 and Wednesday 21 August 2024

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

We will provide an overview of the Medicines Repurposing Program and how interested stakeholders can propose potential new therapeutic uses of existing medicines.

We will provide an overview of the Medicines Repurposing Program and how interested stakeholders can propose potential new therapeutic uses of existing medicines.

Changes to the formatting and structure of the Poisons Standard will come into effect from 1 February 2023