
Australian Register of Therapeutic Goods (ARTG)
The ARTG is the public database of therapeutic goods that can be legally supplied in Australia. You can search the ARTG to find details of therapeutic goods approved for supply.
Searching the Australian Register of Therapeutic Goods (ARTG)
2022年6月21日 · Using the ARTG search function. You can search the ARTG for both medicines and medical devices. Enter your search term into the search box on the TGA website, and you …
Product Information (PI) - Therapeutic Goods Administration (TGA)
2023年2月16日 · You can enter the product name, licence details, sponsor details, active ingredient names or the Australian Register of Therapeutic Goods (ARTG) number to get …
Products we regulate | Therapeutic Goods Administration (TGA)
Australian Register of Therapeutic Goods (ARTG) The ARTG is the public database of therapeutic goods that can be legally supplied in Australia. You can search the ARTG to find details of …
ARTG Search Visualisation Tool - Therapeutic Goods …
This section helps you search ARTG entries by the “ARTG ID, Product Name, Good Name, Sponsor Name, Active Ingredient or Excipient”.
Medicinal cannabis vaping devices that are approved in Australia
There are medicinal cannabis vaping devices included in the Australian Register of Therapeutic Goods (ARTG) that have been approved by the TGA for quality, safety and performance. …
Using Global Medical Device Nomenclature (GMDN) terms for …
Guidance to assist sponsors and manufacturers when applying for inclusion in the Australian Register of Therapeutic Goods (ARTG) and selecting a GMDN term.
New ARTG Search tool available for testing | Therapeutic Goods ...
You can use the ARTG to: check if a product (medicine or medical device) is approved for use in Australia by the TGA before you use it; where available, view and download Consumer …
Therapeutic Goods Administration (TGA)
2025年4月3日 · Search the Australian Register of Therapeutic Goods (ARTG) by name, ID or sponsor. Search results from the ARTG include Consumer Medicine Information (CMI) and …
Complying with regulatory requirements for system or procedure …
System or procedure packs are regulated by the Therapeutic Goods Administration (TGA) as single medical devices in their own right and therefore must be included in the Australian …