Events

Advisory Committee on Medical Devices (ACMD) meeting

Advisory Committee on Vaccines (ACV) meeting

Advisory Committee on Medicines (ACM) meeting

Advisory Committee on Biologicals (ACB) meeting

UDI Webinar 16 – Australian UDI update and guest speakers on the value of UDI for procurement and inventory management in hospitals.

Advisory Committee on Complementary Medicines (ACCM) meeting

Advisory Committee on Medical Devices (ACMD) meeting

Advisory Committee on Vaccines (ACV) meeting

Advisory Committee on Medicines (ACM) meeting

The 3rd meeting of the Women's Health Product Working Group (WHPWG #3), March 2023

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

This webinar will address the recent announcement by the TGA that medicines containing psilocybin and MDMA will be conditionally classified as Schedule 8 (controlled drug) in the Poisons Standard.

This webinar will address the recent announcement by the TGA that medicines containing psilocybin and MDMA will be classified as Schedule 8 (controlled drug) when prescribed by a psychiatrist.

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.

Advisory Committee on Medical Devices (ACMD) meeting

Advisory Committee on Vaccines (ACV) meeting

Advisory Committee on Medicines (ACM) meeting

This webinar will explain labelling requirements for finished MCP in detail.

The 2nd meeting of the Women's Health Product Working Group (WHPWG #2), October 2022

Advisory Committee on Vaccines (ACV) meeting

Understand the key findings of the independent expert report on the risks of intentional self-poisoning with paracetamol and have your questions answered about the TGA’s consultation (starting mid-September) on the possible options for changing access or purchasing controls through the Poisons Standard.

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

This webinar will guide you through the process of charging for regulatory activities, the medicinal cannabis funding model and the fees and charges structure and amounts proposed to commence on 1 July 2023.

The final webinar in this series will explore the impact changes to the EU MDR will have on consent to supply and market notifications.

The final webinar in this series will explore the impact changes to the EU MDR will have on consent to supply and market notifications.