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  • Public consultation on proposed amendments to the Poisons Standard - March 2021 ACMS/ACCS meetings

    Scheduling amendments referred to expert advisory committee This pre-meeting consultation is for applications and delegate initiated proposals to amend the scheduling in the Poisons Standard for certain substances. The scheduling amendments and any submissions received will be considered at either the meeting of the Advisory Committee on Medicines Scheduling (ACMS) , meeting of the Advisory Committee on Chemicals Scheduling (ACCS) , or a... More
    Opened 24 December 2020

  • SURVEY: Personalised medical devices - further resources for stakeholders

    From 25 February 2021, a new framework for regulating personalised medical devices will commence. Comprehensive guidance about the framework can be found at: https://www.tga.gov.au/resource/personalised-medical-devices-including-3d-printed-devices The Therapeutic Goods Administration (TGA) is conducting an education campaign to help stakeholders to understand the new framework and meet their regulatory obligations, ensuring minimal interruption to the supply of personalised... More
    Opened 14 December 2020

  • Medicinal Cannabis Permit Reform

    The Department of Health through the Office of Drug Control (ODC) is seeking comments from interested parties on a review of the structure, design and administrative processes for medicinal cannabis related permits (the review). This review is part of the broader reforms being implemented as a result of the statutory Review of the Narcotic Drugs Act 1967 undertaken in 2019 by Professor John McMillan AO. More
    Opened 11 November 2020

  • TGA's New Post Market Review Compliance Dashboard

    From 19 October 2020, how the TGA engages with the sponsors for post market reviews has changed. A new medical device Post Market Review Compliance Dashboard has been developed in TBS to respond to post market reviews. The new compliance dashboard will provide the sponsors with an efficient and secure way of responding to post market reviews. The purpose of this survey is to seek your feedback on the new Post Market Review Compliance Dashboard. More
    Opened 8 November 2020

  • Impact of amendments to the application process for inclusion of Class I medical devices in the Australian Register of Therapeutic Goods (ARTG)

    The Australian Government is undertaking a significant program to reform the regulation of therapeutic goods in Australia. As part of the Australian Government Department of Health, the Therapeutic Goods Administration (TGA) regulates therapeutic goods, and is responsible for implementing the Government’s reforms. The TGA has issued this survey as part of the Government’s reform program. The purpose of this survey is to seek your feedback on the amendments to the application... More
    Opened 15 October 2020

  • Compounded medicines and good manufacturing practice (GMP)

    The current guidance Compounded medicines and good manufacturing practice (GMP) was developed in relation to the PIC/S Guide to GMP for Medicinal Products PE-009-8 15 January 2009, following public consultation in 2015. This document provides guidance on the interpretation of the PIC/S Guide to GMP for manufacturers licenced by the TGA to manufacture compounded and dispensed therapeutic goods. Following the adoption by the TGA of the PIC/S Guide to GMP PE009-14 as the Manufacturing... More
    Opened 1 October 2020

  • Notice of an interim decision to amend the current Poisons Standard in relation to nicotine - Joint ACMS-ACCS meeting, June 2020

    Interim decision to amend the current Poisons Standard in relation to nicotine, Joint ACMS-ACCS meeting #25, June 2020 This consultation is for an interim decision to amend the scheduling of nicotine in the current Poisons Standard, following advice sought at the 23 June 2020 meeting of the Advisory Committee on Medicines and Chemicals Scheduling in joint session (Joint ACMS-ACCS #25, June 2020). The interim decision on nicotine scheduling is a separate process... More
    Opened 23 September 2020

  • Exploring options for the introduction of an Australian Unique Device Identification (UDI) System: UDI consultation paper 2

    The Australian Government is undertaking a significant program of reform to the regulation of therapeutic goods in Australia. As part of the Australian Government Department of Health, the Therapeutic Goods Administration (TGA) regulates therapeutic goods, and is responsible for implementing the Government’s reforms. We have issued this consultation paper as part of the reform program. This is the second consultation paper published by the TGA relating to the proposed... More
    Opened 23 September 2020

  • Proposed Enhancements to Adverse Event Reporting for Medical Devices - Industry

    The Australian Government is undertaking a significant program to reform the regulation of therapeutic goods in Australia. As part of the Australian Government Department of Health, the Therapeutic Goods Administration (TGA) regulates therapeutic goods, and is responsible for implementing the Government’s reforms. The TGA has issued this consultation paper as part of the Government’s reform program . The purpose of this consultation paper is to seek feedback on proposals... More
    Opened 23 September 2020

  • Proposed Enhancements to Adverse Event Reporting for Medical Devices - Consumers

    The Australian Government is undertaking a significant program to reform the regulation of therapeutic goods in Australia. As part of the Australian Government Department of Health, the Therapeutic Goods Administration (TGA) regulates therapeutic goods, and is responsible for implementing the Government’s reforms. The TGA has issued this consultation paper as part of the Government’s reform program. The purpose of this consultation paper is to seek feedback on proposals that aim... More
    Opened 23 September 2020

  • NOTIFICATION FORM: Transition arrangements for medical devices that record patient images, and anatomical models

    This form should be used by manufacturers and sponsors of medical devices that record patient images or that are anatomical models, and that will be reclassified by the amendments to the Therapeutic Goods (Medical Devices) Regulations 2002 from 25 February 2021. Devices are eligible for transition if: they are medical devices intended to record patient images that are acquired using a method that relies on energy outside the visible spectrum; or they... More
    Opened 21 September 2020

  • Notice of interim decisions to amend (or not to amend) the current Poisons Standard - ACMS/ACCS/Joint ACMS-ACCS meeting, June 2020

    Scheduling amendments referred to expert advisory committee This consultation is for interim decisions made in relation to applications and delegate initiated proposals to amend the scheduling in the Poisons Standard, following advice sought at the 23-25 June 2020 meetings of the Advisory Committee on Medicines Scheduling (ACMS) , and the Advisory Committee on Chemicals Scheduling (ACCS) . All submissions received will be... More
    Opened 9 September 2020

  • Consultation on the new Therapeutic Goods Order 106 - Data matrix codes and serialisation of medicines

    The Therapeutic Goods Administration (TGA) is seeking feedback on proposed requirements for serialisation and the use of data matrix codes on the labels of certain medicines in the Australian supply chain. To make sure the standard is clear, meaningful and fit for purpose. We are seeking feedback on its suitability and potential impacts. Therapeutic Goods (Medicines—Standard for Serialisation and Data Matrix Codes) (TGO 106) Order 2020 Guidance for TGO... More
    Opened 2 July 2020

  • TGA SME Assist Workshop: Meeting Your Obligations (Perth)

    Navigating the re gulatory maze can be a challenge, especially if you're new to regulation. SME Assist in partnership with The Western Australian Health Translation Network presents Meeting Your Obligations: a free workshop aimed at beginners who are unfamiliar with therapeutic goods regulation. This may include: small to medium enterprises (SMEs) start-ups researchers If you are making therapeutic claims about a product or... More
    Opened 12 August 2019

  • GMP Forum 2018 - Survey

    TGA Conference Evaluation online form 2018 GMP Forum 26 June 2018 More
    Opened 28 June 2018

  • AusPAR Survey

    The TGA would like to know what you think about the Australian Public Assessment Reports (AusPARs) for prescription medicines. This questionnaire should only take a couple of minutes to complete and will help us to understand who the audience of an AusPAR is, what AusPARs are used for and how useful their content is to our external stakeholders. More
    Opened 2 May 2016

  • Questionnaire for continuing panel members

    We want to know what you think about the TGA so we can enhance our support for all panel members. This questionnaire should only take you about 7-10 minutes to complete. The questionnaire focuses on key issues such as: the quoting process administrative correspondence the guidance and direction received from the TGA delegate interaction with the TGA during the evaluation phase; and TGA feedback. Responses to this questionnaire will be used... More
    Opened 10 December 2014
137 results. Page 5 of 5