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BioWorld - Thursday, June 18, 2026
Home » Topics » Regulatory » TGA

TGA
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TGA: More feedback needed on repurposing drugs

March 10, 2022
By Mari Serebrov
Given the challenges in repurposing medicines, Australia’s Therapeutics Goods Administration (TGA) opened a second consultation on the subject March 10.
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Flag of Australia, sky background

Companies favor mandatory reporting of device-related adverse events, wary of data integrity

Feb. 25, 2022
By Tamra Sami
PERTH, Australia – Nearly three-fourths of medical device stakeholders supported introducing mandatory reporting of medical device-related adverse events by health care facilities in Australia, but many raised concerns about data duplication and integrity.
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Gavel and stacks of coins

Australia’s TGA to increase industry fees to retain its cost recovery model

Feb. 1, 2022
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Good Administration (TGA) plans to increase all fees and charges to industry by 2.6% for the 2022 to 2023 financial year, and it is seeking feedback on proposed options.
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Gavel and stacks of coins

Australia’s TGA to increase industry fees to retain its cost recovery model

Jan. 27, 2022
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Good Administration (TGA) plans to increase all fees and charges to industry by 2.6% for the 2022 to 2023 financial year, and it is seeking feedback on proposed options.
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Map of Australia, vaccine vial and syringe

Australia adds Novavax vaccine and antivirals from Pfizer, MSD to COVID-19 arsenal

Jan. 25, 2022
By Tamra Sami
PERTH, Australia – In preparation for easing COVID-19 restrictions and opening its international borders, Australia has added a new vaccine and two new oral antiviral therapies to its arsenal to fight the omicron variant of the SARS-CoV-2 virus that is sweeping the globe. Australia’s Therapeutic Goods Administration granted provisional approval on Jan. 20 to Biocelect Pty Ltd. (on behalf of Novavax Inc.) for its COVID-19 vaccine, Nuvaxovid, as well as two oral antiviral treatments.
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Map of Australia, vaccine vial and syringe

Australia adds Novavax vaccine and antivirals from Pfizer, MSD to COVID-19 arsenal

Jan. 25, 2022
By Tamra Sami
PERTH, Australia – In preparation for easing COVID-19 restrictions and opening its international borders, Australia has added a new vaccine and two new oral antiviral therapies to its arsenal to fight the omicron variant of the SARS-CoV-2 virus that is sweeping the globe. Australia’s Therapeutic Goods Administration granted provisional approval on Jan. 20 to Biocelect Pty Ltd. (on behalf of Novavax Inc.) for its COVID-19 vaccine, Nuvaxovid, as well as two oral antiviral treatments.
Read More
Map of Australia, vaccine vial and syringe

Australia adds Novavax vaccine and antivirals from Pfizer, MSD to COVID-19 arsenal

Jan. 20, 2022
By Tamra Sami
PERTH, Australia – In preparation for easing COVID-19 restrictions and opening its international borders, Australia has added a new vaccine and two new oral antiviral therapies to its arsenal to fight the omicron variant of the SARS-CoV-2 virus that is sweeping the globe. Australia’s Therapeutic Goods Administration granted provisional approval on Jan. 20 to Biocelect Pty Ltd. (on behalf of Novavax Inc.) for its COVID-19 vaccine, Nuvaxovid, as well as two oral antiviral treatments.
Read More
Australian flag on laptop screen with health professional

TGA issues guidance on software requirements for COVID-19 rapid antigen self-tests

Jan. 12, 2022
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Goods Administration (TGA) released guidance for sponsors and manufacturers on regulatory requirements for software to be used with COVID-19 rapid antigen self-tests that are intended to analyze and interpret tests results.
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Flag of Australia, sky background
MTAA annual conference

Australia’s device reforms mostly completed, but postmarketing efforts take central stage

Dec. 31, 2021
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Goods Administration (TGA) has undertaken a massive effort to reform its drug and device regulations, and as it pulls into the homestretch with those reforms, it is setting its sights to postmarketing efforts that include adverse event reporting, conformity assessments, patient-reported outcomes and a universal device identifier program.
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Woman holding smartphone coughing

Resapp’s stand-alone cough counter app cleared in Australia and Europe

Dec. 29, 2021
By Tamra Sami
PERTH, Australia – Australian digital health company Resapp Health Ltd. received clearance from Australia’s Therapeutics Good Administration and CE mark certification in the EU for its stand-alone cough counter application that tracks cough frequency using a smartphone. The class I software as a medical device is the first regulatory approval for such an application, which uses Resapp’s machine learning algorithms to identify cough events from audio recorded using the smartphone’s in-built microphone.
Read More
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