Looking for Expert Regulatory Affairs Services Provider in Australia? The Therapeutic Goods Administration (TGA) of Australia plays a critical role in ensuring the quality, safety, and efficacy of medicinal products and medical devices in the country. As one of the key regulatory authorities, the TGA mandates that all medicinal products, including devices, must be listed, registered, or included on the Australian Register of Therapeutic Goods (ARTG) unless exempted. The ARTG serves as a comprehensive database, listing essential details like product names, active ingredients, categorization, sponsors, and manufacturers.