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567 result(s) found, displaying 551 to 567
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Meeting statementsSummary to provide advice of the Resolutions made by the Therapeutic Goods Committee at its 29th Meeting held on 7 September 2006
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Meeting statementsSummary to provide advice of the Resolution made by the Therapeutic Goods Committee (TGC) out-of-session during April 2006
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Meeting statementsSummary to provide advice of the Resolutions made by the Therapeutic Goods Committee at its 28th Meeting held on 24 January 2006
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Meeting statementsSummary to provide advice of the Resolutions made by the Therapeutic Goods Committee at its 27th Meeting held on 9 June 2005
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Meeting statementsSummary to provide advice of the Resolution made by the Therapeutic Goods Committee (TGC) out-of-session during April 2005
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Meeting statementsSummary to provide advice of the Resolutions made by the Therapeutic Goods Committee at its 26th Meeting held on 24 November 2004
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Meeting statementsSummary to provide advice of the Resolutions made by the Therapeutic Goods Committee at its 25th Meeting held on 7 September 2004
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Corporate reports
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Meeting statementsSummary to provide advice of the Resolutions made by the Therapeutic Goods Committee at its 24th Meeting held on 4 May 2004
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Meeting statementsSummary to provide advice of the Resolution made by the Therapeutic Goods Committee (TGC) out-of-session during February 2004
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Meeting statementsSummary to provide advice of the Resolutions made by the Therapeutic Goods Committee at its 23rd Meeting held on 17 December 2003
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Meeting statementsSummary to provide advice of the Resolutions made by the Therapeutic Goods Committee at its 22nd Meeting held on 11 August 2003
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Meeting statementsSummary to provide advice of the Resolutions made by the Therapeutic Goods Committee at its 21st Meeting held on 11 February 2003
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Meeting statementsSummary to provide advice of the Resolutions made by the Therapeutic Goods Committee at its 20th Meeting held on 16 April 2002
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Meeting statementsSummary to provide advice of the Resolutions made by the Therapeutic Goods Committee at its 19th Meeting held on 8 November 2001
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Corporate reportsThe IRIS is responsible for the management of all reports of adverse events or problems associated with medical devices that are reported to the TGA.
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Corporate reportsNote for guidance on clinical safety data management: definitions and standards for expedited reporting