ARTGAustralian Register of Therapeutic Goods
ARTGAnti-Rabbit Thymocyte Gammaglobulin
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TheTGA has implemented a new assessed listed medicines pathway for sponsors to enter certain complementary medicines on the ARTG:
There was significant difference (p<0.05) noted after 06 weeks of training in ARTG as compared to TOTG.
The Konecranes ARTG system is built around Konecranes' market-leading 16-wheel RTG, which has a unique ability to tolerate rough yard surfaces.
Here the authors review the regulatory requirements of CAMS (with details of registered vs listed goods, government fees and charges, and the TGA Advertising Code); compare weight-loss products listed on the Australian Register of Therapeutic Goods (ARTG) (publically available) with registered pharmaceutical products; analyse complaint procedures and advocate policy change.
This approval allows the product to be used in sunscreens and other non-prescription products which are proposed for registration or listing in the Australian Register of Therapeutic Goods (ARTG).
The TGA maintains the Australian Register of Therapeutic Goods (ARTG)--a database of information about therapeutic goods approved for use in or export from Australia.
ATG (Art Technology Group, Inc., Nasdaq: ARTG), provider of an e-business software platform and applications for e-commerce, relationship management, and portals, recently announced its plans to support the deployment of the ATG Dynamo e-Business Platform and its enterprise applications on the Oracle9i Application Server in 2002.
Konecranes recently introduced in the container-handling industry its automated rubber tyred gantry (ARTG) system which the company says provides RTG terminal operators with all the benefits of automation: operational cost savings, greater productivity, increased predictability and increased safety.
More recently there has been a listing of registered CM products, The Australian Register of Therapeutic Goods (ARTG.) The TGA will also be compiling an electronic listing of products for users, enhancing sanctions and penalties for breaches of compliance, and enforcing changes to explanations on labels to encourage transparency.
EnteroMedics said, that in addition to receiving the previously announced initial approvals for the critical active implantable medical device (AIMD) components of the Maestro System by the Therapeutic Goods Administration (TGA) for the listing on the Australian Register of Therapeutic Goods (ARTG), it has also received approval for six of the eight remaining individual class III components.
In Australia, proposed reforms to the medical device regulatory system also will amend the existing Australian Register of Therapeutic Goods (ARTG) database.