What does ARTG mean in THERAPEUTICS
The Australian Register of Therapeutic Goods (ARTG) is a register of all therapeutic goods that have been approved for marketing in Australia. It is maintained by the Therapeutic Goods Administration (TGA), a division of the Australian Department of Health. The ARTG provides the public with information about therapeutic goods, such as safety and efficacy data, product descriptions and contact details for manufacturers and suppliers. It also lists products that are not allowed to be sold in Australia due to safety or other concerns. The purpose of the ARTG is to protect the public from potential risks associated with therapeutic goods, such as serious side effects or contamination.
ARTG meaning in Therapeutics in Medical
ARTG mostly used in an acronym Therapeutics in Category Medical that means Australian Register of Therapeutic Goods
Shorthand: ARTG,
Full Form: Australian Register of Therapeutic Goods
For more information of "Australian Register of Therapeutic Goods", see the section below.
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Essential Questions and Answers on Australian Register of Therapeutic Goods in "MEDICAL»THERAPEUTICS"
What is the Australian Register of Therapeutic Goods?
The Australian Register of Therapeutic Goods (ARTG) is a publicly accessible register established by the Australian Government’s Therapeutic Goods Administration (TGA). It contains information about therapeutic goods that are made available for sale in Australia, including prescription and over-the-counter medicines. The ARTG also includes complementary medicines, medical devices and blood components.
How does a product get listed on the ARTG?
In order for a product to be listed on the ARTG, manufacturers and importers must provide detailed evidence that the product meets safety, quality and efficacy requirements as set out in relevant legislation. This includes submitting clinical trials or other evidence to demonstrate that the product works as claimed.
What benefits come with inclusion on ARTG?
By listing products on the ARTG, manufactures and importers are eligible to apply for reimbursement through national health schemes such as Medicare Benefits Schedule and Pharmaceutical Benefits Scheme. In addition, inclusion on ARTG can help foster trust in therapeutic goods among consumers due to greater transparency of information about them.
Are all therapeutic products required to be included on ARTG?
Yes. All medicines, medical devices and related components sold in Australia must be included on the ARTG before they can be made available for sale. This includes manufacturing or importing into Australia from another country as well as advertising them for sale.
Who oversees operations at ARTG?
The Australian government's Therapeutic Goods Administration (TGA) has oversight over operations at the Australian Register of Therapeutic Goods (ARTG). The TGA is responsible for ensuring that therapeutic goods are safe and effective prior to being registered and marketed within Australia.
Can I access information stored in the ARTG register?
Yes – Some information stored in the ARTG register is publicly accessible. This includes basic details regarding therapeutic goods such as their name, sponsor company name and date of registration among others. Detailed information such as clinical trial data or adverse events reports may not be publicly viewable depending on privacy settings established by their respective sponsors.
Does every therapeutic product need an entry in the ARTG register?
Yes – Every therapeutic product needs an individual entry in order to be legally marketed within Australia, including repeat prescriptions which require a separate entry each time it is dispensed even if it was previously entered onto the register with identical characteristics.
How do I know if my medicine has been registered with TGA?
You can check whether your medicine has been registered using Check Medicine by entering either your medicine’s brand name or active ingredient(s). Alternatively you can search via manufacturer's name using Search Manufacturers facility provided by TGA website.
Final Words:
In summary, the Australian Register of Therapeutic Goods (ARTG) is an important tool used by TGA to ensure that only safe and effective therapeutic goods are available on the market in Australia. All manufacturers must register their product with TGA and submit evidence supporting its safety before it can be listed on the ARTG. By monitoring changes in product ingredients or manufacturing methods regularly according to current regulations set by TGA – consumers can confidently purchase products knowing that they meet industry standards for quality control.