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  • 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
    Closed 23 December 2014
  • 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
    Closed 31 July 2016
  • GMP Forum 2018 - Survey

    TGA Conference Evaluation online form 2018 GMP Forum 26 June 2018 More
    Closed 8 July 2018
  • 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
    Closed 13 September 2019
  • 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
    Closed 20 August 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
    Closed 13 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
    Closed 12 November 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
    Closed 18 December 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
    Closed 18 December 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
    Closed 24 December 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
    Closed 24 December 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
    Closed 24 December 2020
  • 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
    Closed 27 January 2021
  • Consultation: Australian Medical Device Regulations definition of Central Circulatory System (CCS)

    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. In 2019, the TGA consulted on changes to the classification rules in Proposed changes to the... More
    Closed 10 February 2021
  • Agent access to notifications on Post Market Review Medical Devices Compliance dashboard

    From 19 October 2020, the process by which the Therapeutic Good Administration (TGA) engages with the sponsors 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 is providing the sponsors with an efficient and secure way of responding to post market reviews. At present, the Post Market Review Medical Devices Compliance portal does not grant access to... More
    Closed 17 February 2021
  • Removing redundant processes for entering certain formulation information into a therapeutic goods application

    The Therapeutic Goods Administration (TGA) is seeking feedback on a proposal to streamline how information about certain therapeutic goods formulations is entered into TGA electronic systems when seeking market approval. Specifically, we propose to discontinue entering certain types of formulations into a subordinate database of ingredient mixtures (known as the Proprietary Ingredients Table) before they are selected into therapeutic goods applications for inclusion in the ... More
    Closed 24 February 2021
  • Public consultation on interim decisions to amend the Poisons Standard - November 2020 ACMS/ACCS meetings

    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 Poisons Standard, following advice sought at the 4-5 November 2020 meetings of the Advisory Committee on Medicines Scheduling (ACMS) and the Advisory Committee on Chemicals Scheduling (ACCS) . The closing date for this consultation is close of business 4 March 2021 . All submissions received by the... More
    Closed 4 March 2021
  • Public Consultation - Fees and charges proposal 2021-22

    The Therapeutic Goods Administration (TGA) is conducting a public consultation to provide industry and other interested stakeholders with an opportunity to comment on options for the TGA’s proposed fees and charges for the 2021-22 financial year. Specifically, we are seeking feedback on the potential impact/s of the proposed options, prior to seeking approval from the Government for any changes. The Therapeutic Goods Administration (TGA) within the Department of Health is responsible... More
    Closed 17 March 2021
  • Proposal for clarifying regulatory requirements for residual claims for disinfectants

    This consultation is to obtain feedback in relation to proposals to provide clarity on residual claims for disinfectants. The Therapeutic Goods Administration (TGA) has received a number of enquiries relating to residual activity claims for disinfectants, including whether statements can be made for disinfectants such as ‘residual activity for up to 30 days’, and what testing methods should be used to provide evidence for these claims. At present, there is no... More
    Closed 26 March 2021
  • Repurposing of Prescription Medicines

    Repurposing is the process of identifying new uses (or ‘indications’) for medicines. In some cases, prescription medicines may have been used ‘off-label’ for many years to treat conditions that they do not have formal regulatory approval (i.e. are not registered) for. Whilst this may be accepted clinical practice, obtaining formal regulatory approval for the repurposed indication can lead to wider and safer use as it means that the evidence base for such clinical use has been... More
    Closed 30 March 2021
  • TGO 110 – Standard for Vaporiser Nicotine - Consultation

    The Therapeutic Goods Administration (TGA) is seeking comments on a proposed standard for vaporiser nicotine products. Vaporiser nicotine products are nicotine-containing products intended to be used in vaping devices such as e-cigarettes, e-cigars and other electronic nicotine delivery systems (ENDs). This includes vape liquids, e-liquids and e-juices that contain nicotine and/or nicotine salts. This does not include other nicotine replacement therapies (NRTs) containing... More
    Closed 31 March 2021
  • Proposed regulatory options for medical devices containing nanomaterials

    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. In 2015, the Report of the Expert Panel Review of Medicines and Medical Devices Regulation... More
    Closed 9 April 2021
  • Building a more robust medicine supply: proposals to help prevent, mitigate and manage medicine shortages

    The Therapeutic Goods Administration (TGA) is seeking feedback on proposals to help ensure ongoing, reliable supply of important medicines. Medicine shortages have been of particular concern during the COVID-19 pandemic. We have been reviewing the ways in which we can better assist affected Australian patients and their healthcare providers. Specifically, we are seeking feedback on possible reforms that would: prioritise the evaluation and registration process... More
    Closed 17 May 2021
  • Proposed changes to Required Advisory Statements for Medicine Labels (RASML): Menthol

    The Therapeutic Goods Administration (TGA) is seeking comments from interested parties on the addition of proposed new advisory statements for labels of over the counter (OTC) and registered complementary medicines containing menthol for dermal use, for inclusion in the Required Advisory Statements for Medicine Labels (RASML) . The proposal to include advisory statements for menthol in RASML follows previously implemented requirements for advisory statements on labels of... More
    Closed 18 May 2021
  • Proposed changes to Required Advisory Statements for Medicine Labels (RASML): Sedating antihistamines

    The Therapeutic Goods Administration (TGA) is seeking comments from interested parties on changes to current requirements for advisory statements for labels of non-prescription medicines containing antihistamines indicated for short term use in insomnia (diphenhydramine, doxylamine and promethazine), as included in the Required Advisory Statements for Medicine Labels (RASML) document. More
    Closed 18 May 2021
  • Proposed changes to Required Advisory Statements for Medicine Labels (RASML): Lidocaine (lignocaine)

    The Therapeutic Goods Administration (TGA) is seeking comments from interested parties on addition of a proposed new required advisory statement for labels of non-prescription medicines containing more than 1.5 per cent lidocaine (lignocaine) for topical oral use, for inclusion in the Required Advisory Statements for Medicine Labels (RASML) document. The required advisory statement “Do not use for teething pain in children” is proposed for preparations for topical oral... More
    Closed 18 May 2021
  • Proposed changes to Required Advisory Statements for Medicine Labels (RASML): Methyl salicylate

    The Therapeutic Goods Administration (TGA) is seeking comments from interested parties on proposed new advisory statements for labels of over the counter (OTC) and registered complementary medicines containing methyl salicylate for dermal use , for inclusion in the Required Advisory Statements for Medicine Labels (RASML) . The proposal to include advisory statements for methyl salicylate-containing medicines in RASML follows previously implemented requirements for... More
    Closed 18 May 2021
  • Public consultation on proposed amendments to the Poisons Standard (hand sanitisers) - Joint ACMS-ACCS, June 2021

    Scheduling amendments referred to expert advisory committee This consultation is for applications and delegate initiated proposals to amend the Poisons Standard. The scheduling amendments and any submissions received will be considered at the June 2021 joint meeting of the Advisory Committee on Medicines Scheduling (ACMS) and the Advisory Committee on Chemicals Scheduling (ACCS) . The closing date for this consultation is close of business 27 May 2021. ... More
    Closed 27 May 2021
  • Public consultation on proposed amendments to the Poisons Standard - ACMS, June 2021

    Scheduling amendments referred to expert advisory committee This consultation is for applications and delegate initiated proposals to amend the Poisons Standard. The scheduling amendments and any submissions received will be considered at the June 2021 meeting of the Advisory Committee on Medicines Scheduling (ACMS) . The closing date for this consultation is close of business 27 May 2021. All submissions received by the deadline will be considered by... More
    Closed 27 May 2021
  • Public consultation on proposed amendments to the Poisons Standard (sodium nitrite) - Joint ACMS-ACCS, June 2021

    CONTENT WARNING The Department of Health acknowledges the devastating effects associated with acts of self-harm on individuals, their families, friends and communities. This consultation relates to information on self-poisonings that some people may find distressing. If you, or someone you know, is in need of additional support, please contact any of the below crisis support helplines. Support services and information sources Adult Lifeline : 13 11 14 ... More
    Closed 27 May 2021
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