Use the filters below to narrow your search.
Filter results
You can narrow down the results using the filters.
Topic
- Advertising (273)
- COVID-19 (163)
- Safety monitoring and information (97)
- Legislation (93)
- Compliance and enforcement (66)
- Vaping hub (53)
- Manufacturing (52)
- Labelling and packaging (35)
- Scheduling (national classification system) (27)
- Import and export (26)
- Medicinal cannabis hub (25)
- Sunscreens (16)
- Shortages and supply disruptions (14)
- Weight loss products (14)
- Committees and advisory bodies (9)
- Cosmetics (5)
- Unique Device Identification (UDI) hub (4)
- Clinical trials (3)
- Fees and payments (2)
- Prescription opioids hub (2)
- Urogynaecological (transvaginal) surgical mesh hub (2)
- Breast implant hub (1)
Search
1258 result(s) found, displaying 1101 to 1125
-
Media releasesDealing countefeit and unapproved medicines is a serious offence as shown in recent TGA prosecution outcome in South Australia
-
BlogIs there a hangover cure? Essential reading for anyone visited by spirits these holidays.
-
Safety updatesInfliximab and mycosis fungoides, infliximab and lupus-like syndrome, and medicine shortages mandatory reporting
-
Media releasesThis legal action follows an investigation by the Therapeutic Goods Administration
-
Regulatory decision noticesTGO 100 has been registered on the Federal Register of Legislation. It commences on 8 December 2018, repealing and replacing TGO 98
-
Media releasesThere will not be a decision announced on scheduling of alkyl nitrites on 29 November 2018. Further public consultation will be undertaken.
-
News articlesReforms relating to accessing unapproved products include modifications to the Special Access Scheme and Authorised Prescriber scheme to allow streamlined access to certain unapproved therapeutic products.
-
News articlesThe complementary medicine regulatory reforms include changes that will create a new approval pathway for listed complementary medicines and increase availability of information to support consumer decisions.
-
News articlesThe prescription medicines regulatory reforms include changes that will bring medicines to market sooner in Australia, while maintaining a robust framework for safety, quality and efficacy.
-
News articlesReforms to TGA advisory committees include changes that provide greater efficiencies and a reduction in the number of statutory advisory committees that provide independent advice to the TGA.
-
Safety updatesStandards minimise risk of misconnections; eltrombopag interference with test results; amniotic fluid tests
-
News articlesCabozantinib (CABOMETYX) is the first medicine to be registered via the new COR-A pathway
-
BlogWhat is the TGA? Learn why and how we regulate medicines and medical devices.
-
Media releasesJoint media release between Australian Border Force and Therapeutic Goods Administration
-
BlogSome retailers try to use disclaimers like 'for research purposes only' to sell an illegal product, but these disclaimers don't change the law.
-
Safety updatesCase studies in Incident Report Investigations; review of reusable biopsy forceps devices; care required with patient lifters
-
Media releasesThe TGA has launched a web hub to help consumers and health professionals find information on transvaginal (urogynaecological) surgical mesh.
-
Safety updatesNew warning labels for neuromuscular blocking agents; local anaesthetic systemic toxicity; off-label use of atropine
-
BlogGeorgia's story explains how to spot the warning signs for the breast implant associated cancer BIA-ALCL.
-
Regulatory decision noticesTGA issues advertising direction
-
Media releasesToday we celebrate the official launch of the TGA Facebook page
-
Safety updatesThe TGA completed a desktop review of selected listed sunscreen products.
-
Safety updatesBe aware of cross-reactivity with home-use self-test ovulation kits, TGA undertakes product safety review into intragastric balloon systems
-
Media releasesOur annual survey measures satisfaction with a range of services and activities including our role and performance
-
Media releasesApalutamide (Erlyand) is the first medicine approved via ACSS Consortium’s NCE working group