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Publications
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Search
764 result(s) found, displaying 176 to 200
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Scheduling submissionsFind out about public submissions on interim decisions for scheduling matters referred to Advisory Committees meetings, held in March 2023
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Scheduling decisions (final)Stay updated on final decisions for substances referred to the March 2023 ACMS/ACCS meetings.
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Meeting statementsRead the meeting statement from 10 August 2023 meeting of the Advisory Committee on Medical Devices (ACMD).
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Corporate reportsRead our business plan 2023-24 to find out about our strategic priorities and activities.
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Meeting statementsAdvisory Committee on Vaccines meeting statement
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Meeting statementsAdvisory Committee on Medicines meeting statement
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Meeting statementsAdvisory Committee on Biologicals meeting statement
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Meeting statementsAdvisory Committee on Biologicals meeting statement
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Meeting statementsAdvisory Committee on Biologicals meeting statement
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Meeting statementsAdvisory Committee on Biologicals meeting statement
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Scheduling decisions (interim)Interim decisions and invitation for further comment. Closing date: 1 September 2023
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Corporate reportsDocuments released under the FOI Act in the 2022/23 financial year
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Meeting statementsRead key points of discussion from the meeting 11 of the Medical Devices Consumer Working Group (MDCWG).
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Scheduling submissionsFind out about public submissions on scheduling matters referred to Advisory Committees meeting, held in March 2023
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Scheduling submissionsFind out about public submissions on scheduling matters referred to Advisory Committees meetings, held in March 2022.
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Scheduling submissionsFind out about public submissions on interim decisions for scheduling matters referred to Advisory Committees meetings, held in March 2022.
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Scheduling decisions (interim)Interim decisions and invitation for further comment. Closing date: 10 August 2023
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Meeting statementsRead the meeting statement from 8 June 2023 meeting of the Advisory Committee on Medical Devices (ACMD).
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Corporate reportsThis Cost Recovery Implementation Statement provides information on how the TGA, within the Department of Health, implements and cost recovers its regulatory activities.
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Corporate reportsMandatory reporting of medical device adverse events by healthcare facilities has begun, with voluntary reporting from March 2025 to 20 March 2026.
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Meeting statementsAdvisory Committee on Vaccines meeting statement
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Meeting statementsAdvisory Committee on Vaccines meeting statement
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Meeting statementsCommunique from the 3rd meeting of the Women's Health Products Working Group (WHPWG), 27 March 2023
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Meeting statementsAdvisory Committee on Medicines meeting statement
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Meeting statementsAdvisory Committee on Medicines meeting statement