Articles

Medical Devices Safety Update, Volume 2, Number 1, January 2014

The TGA is advising consumers against purchasing or using black salve, red salve or cansema products.

Medicines Safety Update, Volume 4, Number 4, August 2013

THERAPEUTIC GOODS ACT 1989

Undertaking to the Secretary of the Australian Department of Health and Ageing given for the purposes of section 42YL of the Act

Mifepristone and misoprostol can be prescribed in Australia by registered medical practitioners.

Hospital supply departments, health professionals, carers and users should check that male urinal bottles are free of sharp edges, both inside and outside the bottle. Any cracks, chips or sharp edges may injure users.

The TGA Prescription Medicines Streamlined Submissions Process Newsletter [formerly the Prescription medicine BPR update (BPR update)] reports on progress of the streamlined submission process.

Safety advice for health professionals on preventing accidental disconnections of patient lines and medical devices, reducing risk of harm.

The Prescription medicine BPR update (BPR update) reports on progress of the streamlined submission process. Each quarter, an update is provided on the PI/CMI project and the AusPAR project.

The Australian government will introduce a comprehensive package of reforms for Australia's Therapeutic Goods Administration (TGA) to ensure the regulation of medicines and medical devices is more effective and transparent.

The TGA intends to cancel all pain-killers containing dextropropoxyphene - Capadex, Di-Gesic, Doloxene and Paradex - from the Australian Register of Therapeutic Goods (ARTG), from 1 March 2012.

The Australian Customs and Border Protection Service and the Therapeutic Goods Administration have taken part in an international ‘Week of Action’ targeting the online sale of counterfeit and illegal medicines.

Contrary to media reports today, the TGA has not approved the use of Nembutal by Dr Nitschke.

The TGA's Incident Reporting and Investigation Scheme receives reports about the safety and performance of medical devices as part of its ongoing monitoring of products supplied in Australia. As part of this process the TGA has recently reviewed several reports associated with repaired endoscopes. These reports relate to the quality of the repair and the use of unsuitable parts.

The Australian Government today released the report of the Therapeutic Goods Administration (TGA) Transparency Review panel, chaired by Professor Dennis Pearce.

Eight synthetic cannabis-like substances will be classified as prohibited substances throughout Australia from 8 July, Parliamentary Secretary for Health and Ageing, Catherine King, has announced.

Landmark agreement to achieve world standards in therapeutic products
media release, The Hon Julia Gillard MP - Prime Minister of Australia

Professor John Horvath has reviewed the use of influenza vaccines in Australia and our system for reporting adverse events following vaccination.

Australian consumers and health professionals will have more ready access to generic medicines following the passage of legislation through the Senate today.

Therapeutic Goods Administration

The Australian community's access to authoritative information about the safety of medicines and medical devices will be greatly enhanced with the launch today of a revamped Therapeutic Goods Administration (TGA) website.

On 4 May 2011 the TGA is going to launch its new corporate website.

Australia's medicines regulator, the Therapeutic Goods Administration, has today issued precautionary advice to doctors not to give patients a second dose of the vaccine Pneumovax 23 pending completion of an investigation into an increased rate of adverse events in people receiving the vaccine for the second time.

TGA is conducting a panel-led review to explore ways to improve transparency and public engagement in its regulatory work.

The Therapeutic Goods Administration (TGA) officially launched a new organisational structure on 1 July 2010.