Events

A regulatory perspective on the Food-Medicine and Cosmetic-Medicine interfaces

A presentation on the current status of the work to establish the Australian UDI system, and questions and answers.

TGA presentation slides from International Congress of Arthroplasty Registries (11 November 2021).

TGA presentation slides from International Society of Pharmacovigilance Annual Meeting, Victoria (10 November 2021).

The 32nd meeting of the Advisory Committee on Chemicals Scheduling (ACCS #32), November 2021.

The 29th joint meeting of the Advisory Committees on Medicines Scheduling and Chemicals Scheduling (Joint ACMS-ACCS #29), November 2021.

The 36th meeting of the Advisory Committee on Medicines Scheduling (ACMS #36), November 2021.

Advisory Committee on Vaccines (ACV) meeting

SME Assist has now published its online workshop - Meeting Your Obligations - Supplying medicinal cannabis in Australia

Webinar presentation on Practical and clinical experience in the practice of smoking cessation treatments in the UK

A presentation on the role of a UDI Issuing Agency, including project update and Q&A.

The role nicotine vaping products can play in a person's journey to quit

This presentation delivered on behalf of the TGA to the students at the University Technology of Sydney as part of the Master of Pharmacy course

Australian Influenza Vaccine Committee (AIVC) meeting

Advisory Committee on Medicines (ACM) meeting

Advisory Committee on Vaccines (ACV) meeting

TGA presentation slides from Vl all Russia Good Manufacturing Practice (GMP) Conference (22 September 2021).

This session will provide information on the creation of UDIs and the role of an Issuing Agency.

TGA presentation slides from NSW Active MedTech Webinar (8 September 2021).

Advisory Committee on Medicines (ACM) meeting

Advisory Committee on Vaccines (ACV) meeting

Presentation from TGA Transformation Stakeholder Engagement Forums.

The Therapeutic Goods Advertising Consultative (TGACC) meeting, 23 August 2021.

A general overview of contamination control in clean rooms for Biologicals.

Common validation errors observed in the GMP Clearance section.