Prescription medicines
- Draft Standard for the Uniform Scheduling of Medicines and Poisons and Draft Scheduling Policy Framework
13 June 2007 - TGA releases second discussion paper: Improving access to CMI and PI
15 February 2007 - Questions & answers about regulating prescription and over-the-counter medicines
16 October 2006 - Consultation - Microbiological standards for medicines in the Australia New Zealand Therapeutic Products Authority (ANZTPA)
27 July 2006 - TGA releases final report into the review of workflow practices within the Drug Safety and Evaluation Branch (DSEB)
17 July 2006 - Consultation documents released
23 May 2006- Draft Medicines Rule
- Proposed Grouping Order for medicines
- Draft guideline on transition provisions for product licensing
- Draft Administration Rule
- Proposed fees and charges
- Medicine Manufacturing Principles
- Discussion paper - Workflow practices within the Drug Safety and Evaluation Branch (DSEB) of the TGA
- Consultation paper - Pharmacopoeial standards for medicines in the Australia New Zealand therapeutic products agency
- Transition to the joint regulatory scheme for prescription and over-the-counter medicines
- Draft best practice guideline on prescription medicine labelling
- Improving access to prescription medicines information