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400 result(s) found, displaying 376 to 400
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Meeting statementsAdvisory Committee on Medical Devices, Meeting 22 statement
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Meeting statementsAdvisory Committee on Medical Devices, Meeting 21 statement
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Meeting statementsAdvisory Committee on Prescription Medicines, Meeting 304 statement
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Meeting statementsAdvisory Committee on Biologicals (ACB), Meeting 6 statement
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Corporate reportsReporting medical device adverse incidents
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Meeting statementsAdvisory Committee on Biologicals, Meeting 5 statement
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Meeting statementsThe Australian Therapeutic Goods Advisory Council met for the fifth time on 5 August 2014
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Meeting statementsAdvisory Committee on Biologicals, Meeting 4 statement
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Meeting statementsTherapeutic Goods Committee, 20 June 2014, meeting statement
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Meeting statementsAdvisory Committee on Complementary Medicines Meeting 16 meeting statement
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Meeting statementsThe Australian Therapeutic Goods Advisory Council met for the fourth time on 4 February 2014
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Meeting statementsAdvisory Committee on Complementary Medicines Meeting 15 meeting statement
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Meeting statementsAdvisory Committee on Biologicals, Meeting 3 statement
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Meeting statementsTherapeutic Goods Committee, 27 August 2013, meeting statement
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Meeting statementsThe Australian Therapeutic Goods Advisory Council met for the third time on 6 August 2013
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Meeting statementsAdvisory Committee on Complementary Medicines Meeting 14 meeting statement
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Meeting statementsAdvisory Committee on Biologicals, Meeting 2 statement
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Meeting statementsAdvisory Committee on Complementary Medicines Meeting 13 meeting statement
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Meeting statementsAustralian Therapeutic Goods Advisory Council met for the second time on 5 February 2013
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Meeting statementsAdvisory Committee on Complementary Medicines Meeting 12 meeting statement
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Meeting statementsThe Australian Therapeutic Goods Advisory Council held its inaugural meeting on 22 November 2012
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Meeting statementsAdvisory Committee on Complementary Medicines Meeting 11 meeting statement
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Meeting statementsAdvisory Committee on Complementary Medicines, Meeting 10 minutes
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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