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22 result(s) found, displaying 1 to 22
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Meeting statementsRead the meeting statement from 8 February 2024 meeting of the Advisory Committee on Medical Devices (ACMD).
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Meeting statementsRead the meeting statement from 7 December 2023 meeting of the Advisory Committee on Medical Devices (ACMD).
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Meeting statementsRead the meeting statement from 12 October 2023 meeting of the Advisory Committee on Medical Devices (ACMD).
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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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Meeting statementsRead the meeting statement from 8 June 2023 meeting of the Advisory Committee on Medical Devices (ACMD).
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Meeting statementsMeeting statement from the Advisory Committee on Medical Devices (ACMD), 13 April 2023.
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Meeting statementsMeeting statement from the Advisory Committee on Medical Devices (ACMD), 9 February 2023.
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Meeting statementsA meeting statement from the fourth meeting of the Dental Sector Working Group is now available.
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Meeting statementsA meeting statement from the third meeting of the Dental Sector Working Group is now available.
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Meeting statementsMeeting statement from meeting 5 of the MDCWG.
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Meeting statementsMeeting statement from meeting 6 of the MDCWG.
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Meeting statementsA meeting statement from the second meeting of the Dental Sector Working Group is now available.
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Meeting statementsDetails for meeting 1 of Australian Dental Sector Working Group held on 19 April 2021.
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Meeting statementsDetails about meeting 1 for the medical device reform consumer working group held in 2019.
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Meeting statementsDetails about meeting 2 for the medical device reform consumer working group held in 2020.
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Meeting statementsDetails about meeting 3 for the medical device reform consumer working group held in 2020.
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Meeting statementsDetails about meeting 4 for the medical device reform consumer working group held in 2020.
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Corporate reportsGuidance for reducing assessment fees for ARTG application audits and TGA conformity assessments of medical devices (including IVDs).
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Corporate reportsDescribers the interaction, role and responsibilities of the TGA and NATA in relation to the regulation of in-house IVDs
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Corporate reportsThis statement guides decision making to help address concerns with joint replacement prostheses.
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Corporate reportsFind out when software is classified as an in vitro medical device and how it is regulated.
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Corporate reportsThe use Global Medical Device Nomenclature (GMDN) codes for in vitro diagnostic medical devices supplied in Australia.