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98 result(s) found, displaying 26 to 50
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ConsultationThis consultation closed on 29 April 2013.
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ConsultationConsultation: Changes to premarket assessment requirements for medical devices: Proposal paper
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ConsultationANZTPA implementation - Release of high level description of a possible joint regulatory scheme
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ConsultationConsultation on proposed advisory statements. Closing date: 7 December 2012
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Corporate reportsARGMD landing page updated with links to new guidance.
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ConsultationConsultation on proposed advisory statements. Closing date: 4 June 2012
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ConsultationConsultation on discussion paper. Closing date: 17 December 2010
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ConsultationThe TGA updated its sunscreen guidelines and related legislation to align with the 2012 Australian/New Zealand Sunscreen Standard, improving clarity, labelling, and regulatory consistency for listed sunscreen products.
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ConsultationFrom 1-21 June 2009 the TGA conducted an online survey of stakeholders seeking feedback on satisfaction in relation to the effectiveness of the TGA's communication and consultation processes.
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ConsultationThis consultation closed on 31 March 2009.
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ConsultationThis consultation closed on 27 March 2009.
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Media releasesInformation about the TGA operations over the 2015/16 Christmas/New Year period
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ConsultationThis consultation closed on 5 September 2008.
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ConsultationThis consultation opened on 10 July 2008 and closed on 15 August 2008.
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Media releasesStage two report for the Review of Medicines and Medical Devices has been released
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Media releasesThe Therapeutic Goods Administration has published an interim decision on a proposal to up-schedule codeine
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Media releasesThe TGA has imposed two new conditions on the inclusion of the SynchroMed II Programmable Pump in the Australian Register of Therapeutic Goods
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ConsultationThis consultation opened on 21 December 2007 and closed on 15 February 2008.
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Media releasesFrom 1 July 2015 commercial IVD medical devices will be monitored under the Regulatory Compliance Framework
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Media releasesFrom 1 July 2015, new guidance and forms for Additional trade names and Extensions of Indications applications will be available
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Media releasesWe have launched the upgraded TGA Business Services site - an improved way to help industry do business with the TGA.
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Media releasesThe TGA is aware of regulatory action undertaken by the US Food and Drug Administration (FDA) in relation to the Maquet manufacturing facility in Hudson, New Hampshire, USA
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Media releasesNext Tuesday we will be launching the new TGA Business Services site.
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Corporate reportsThe Scheduling Policy Framework (SPF) is a key feature of the revised arrangements for scheduling of medicines and chemicals
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Media releases