Consultations
Current consultations
- Nil
Closed consultations
- Stakeholder consultation programme 2006/07
- Proposed Medicine Label Statements – released for stakeholder consultation
Closed 18 August 2007 - Draft Standard for the Uniform Scheduling of Medicines and Poisons and Draft Scheduling Policy Framework
Closed 25 July 2007 - Draft Order: Medical Device Standards for Medical Devices Required to be Sterile
Closed 13 July 2007 - Draft Order: Conformity Assessment Standard for Quality Management Systems and Quality Assurance Techniques for the Manufacture of Medical Devices
Closed 13 July 2007 - Draft Order: Packaging Requirements for Specified Therapeutic Products
Closed 13 July 2007 - Phase 3 ANZTPA consultation documents released
Closed 13 June 2007- In-Vitro Diagnostic Devices (IVD) Revision Draft of the proposed Australia New Zealand Therapeutic Products Regulatory Scheme (Medical Devices) Rule 2007
- Consultation Paper: The Regulation of Human Cellular and Tissue Therapies (HCTs)
- Draft Order: Medical Device Standards for Clinical Evidence
Closed 4 May 2007 - Draft Order: Medical Device Standards for Risk Management
Closed 4 May 2007 - Draft Order: Conformity Assessment Standards for Quality Assurance Techniques for Animal Tissues and their Derivatives Utilised in the Manufacture of Medical Devices
Closed 4 May 2007 - Consultation paper on the proposed clinical trial regulatory arrangements under ANZTPA
Closed 18 April 2007 - TGA releases second discussion paper: Improving access to CMI and PI
Closed 30 March 2007 - Further Phase 2 ANZTPA consultation document released
Closed 14 March 2007- Draft Advertising Rule
- Second phase of ANZTPA consultation documents released
Closed 6 December 2006- Proposed medicines scheduling provisions of the draft Australia New Zealand Therapeutic Products Regulatory Scheme (Administration and Interpretation) Rule 2006
- Consultation Paper on the proposed regulation of Blood under ANZTPA
- Consultation Paper on Product Vigilance in ANZTPA
- Accompanying resource documents
- Microbiological standards for medicines in the Australia New Zealand Therapeutic Products Authority (ANZTPA)
Closed 15 September 2006 - Labelling requirements for medicines under the Australia New Zealand Therapeutic Products Authority - Report on stakeholder consultation and Revised Draft Managing Director's Order
Closed 22 August 2006 - Consultation documents released
Closed 15 August 2006- Draft Medicines Rule
- Proposed Grouping Order for medicines
- Draft guideline on transition provisions for product licensing
- Draft Medical Devices Rule
- Draft Administration Rule
- Proposed fees and charges
- Information sessions on the proposed regulation of homoeopathic and anthroposophic medicines, and essences, in the Australia New Zealand Therapeutic Products Authority (ANZTPA)
Held 11 & 13 July 2006 - Consultation hui
Held 10 July 2006 - Australia and New Zealand Therapeutic Products Authority stakeholder information meetings
Held June 2006 - Meeting for New Zealand manufacturers of prescription and non-prescription medicines, complementary medicines and medical devices
Held 9 June 2006 - Child-resistant packaging requirements for therapeutic goods
Closed 19 May 2006 - Discussion paper: Workflow practices within the Drug Safety and Evaluation Branch (DSEB) of the TGA
Closed 20 January 2006 - Pharmacopoeial standards for medicines in the Australia New Zealand therapeutic products agency
Closed 14 October 2005 - A proposed new model for the scheduling of medicines and poisons within the Joint Agency (TGA Internet site)
Closed 9 September 2005 - Australian review of policy framework for regulating products at the cosmetic/therapeutic interface
Closed 5 May 2005 - Regulatory arrangements for clinical trials and access to unapproved therapeutic products
Closed 8 July 2005 - Improving access to prescription medicines information
Closed 27 June 2005 - Draft labelling requirements for medicines under a joint Australia New Zealand therapeutic products agency
Closed 17 June 2005 - Draft best practice guideline on prescription medicine labelling
Closed 17 June 2005 - Proposed regulatory definitions for complementary medicines and homoeopathic medicines in a joint Australia New Zealand therapeutic products agency
Closed 11 March 2005 - Regulation of herbal substances in a joint Australia New Zealand therapeutic products agency
Closed 11 March 2005 - Regulation of homoeopathic and related medicines in a joint Australia New Zealand therapeutic products agency
Closed 11 March 2005 - Complementary medicines - Permitted ingredients list project
Closed 30 April 2004 - A proposal for a trans Tasman agency to regulate therapeutic products
Closed 2 August 2002 - A possible framework for a joint trans-tasman agency to regulate therapeutic goods (including New Zealand healthcare products)
Closed 2 August 2000