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Half-yearly performance reports - July to December 2013 (TGA - Therapeutic...

(Source: TGA - Therapeutic Goods Administration) 28 May 2014 The TGA prepares statistical performance reports that are presented biannually to the Therapeutic Goods Industry Consultative...

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Safety review of diclofenac (TGA - Therapeutic Goods Administration)

(Source: TGA - Therapeutic Goods Administration) Version 2.1, October 2014 7 October 2014 Following the cardiovascular safety review of all NSAIDs and concerns regarding the...

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Review of cardiovascular safety of non-steroidal anti-inflammatory drugs (TGA...

(Source: TGA - Therapeutic Goods Administration) Version 2.1, October 2014 7 October 2014 A review has been carried out of the relevant medical literature published since 2005 and other relevant data...

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TGA key performance indicators: January to June 2014 (TGA - Therapeutic Goods...

(Source: TGA - Therapeutic Goods Administration) Version 1.0, August 2014 Version history Version Description of change Author Effective date V1.0 Original publication TGA August 2014 TGA key...

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Regulation impact statement: Premarket assessment requirements for Australian...

(Source: TGA - Therapeutic Goods Administration) 15 October 2014 This Regulation Impact Statement (RIS) has been prepared by the Therapeutic Goods Administration (TGA). The purpose is to assist...

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Required advisory statements for medicine labels (RASML) (TGA - Therapeutic...

9 November 2012 The RASML document is a compilation of all mandatory medicine label advisory statements, including those from the Standard for the Uniform Scheduling of Drugs and Poisons (SUSDP) and...

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Documents released under Section 11C of the Freedom of Information Act 1982...

(Source: TGA - Therapeutic Goods Administration) Related information *Large file warning:Attempting to open large files over the Internet within the browser window may cause problems. It is strongly...

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Inaccuracies in clinical trial statistics reporting for the period 2009-2012...

(Source: TGA - Therapeutic Goods Administration) 1 August 2013 The Therapeutic Goods Administration (TGA) has identified errors in its internal reports of clinical trial numbers for the period 1 July...

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Consultation: Draft OTC medicine monograph for guaifenesin (TGA - Therapeutic...

(Source: TGA - Therapeutic Goods Administration) 12 September 2014 Closing date: 10 October 2014 Invitation to comment The TGA is seeking comments from interested parties on the draft OTC medicine...

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Consultation: Draft OTC medicine monograph for mebendazole (TGA - Therapeutic...

(Source: TGA - Therapeutic Goods Administration) 12 September 2014 Closing date: 10 October 2014 Invitation to comment The TGA is seeking comments from interested parties on the draft OTC medicine...

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Consultation: Draft OTC medicine monograph for ranitidine hydrochloride (TGA...

(Source: TGA - Therapeutic Goods Administration) 12 September 2014 Closing date: 10 October 2014 Invitation to comment The TGA is seeking comments from interested parties on the draft OTC medicine...

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Consultation: Draft OTC medicine monograph for loperamide hydrochloride (TGA...

(Source: TGA - Therapeutic Goods Administration) 12 September 2014 Closing date: 10 October 2014 Invitation to comment The TGA is seeking comments from interested parties on the draft OTC medicine...

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Consultation: Medicine labelling (TGA - Therapeutic Goods Administration)

(Source: TGA - Therapeutic Goods Administration) 22 August 2014 Closing date: 7 October 2014 Invitation to comment The TGA is seeking comments from interested parties on any, or all, of the proposed...

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Consultation: Permitted (coded) indications for listed medicines (TGA -...

(Source: TGA - Therapeutic Goods Administration) 14 January 2013 Closing date: Friday 15 March 2013 Consultation documents Consultation: Permitted (coded) indications for listed medicines Consultation:...

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Consultation: Changes to premarket assessment requirements for medical...

(Source: TGA - Therapeutic Goods Administration) Closing date: Friday 15 March 2013 Consultation documents * Changes to premarket assessment requirements for medical devices: Proposal paper (Microsoft...

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Consultation principles for therapeutic goods regulatory reforms (TGA -...

(Source: TGA - Therapeutic Goods Administration) Your browser appears to have JavaScript disabled. The TGA mobile website works best with JavaScript enabled. 21 June 2013 We have...

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Consultation: Review of cardiovascular safety of non-steroidal...

(Source: TGA - Therapeutic Goods Administration) 7 October 2014 Closing date: 6 November 2014 Invitation to comment The TGA is seeking comments from interested parties following a Review of...

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Consultation: Loratadine and desloratadine: proposed advisory statements for...

Version 1.0 9 November 2012 Closing date: 7 December 2012 Invitation to comment The TGA is seeking comments from interested parties on the proposed advisory statement for loratadine and desloratadine...

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Australian Therapeutic Goods Advisory Council (TGA - Therapeutic Goods...

(Source: TGA - Therapeutic Goods Administration) 16 January 2013 Introduction On 16 July 2012, the Australian Government announced that it would establish an Australian Therapeutic Goods Advisory...

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TGA reforms: A blueprint for TGA's future: Progress report as at 30 June 2014...

(Source: TGA - Therapeutic Goods Administration) 25 September 2014 TGA reforms: A blueprint for TGA's future - Progress report as at 30 June 2014 is the fourth six monthly progress report on reforms...

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