This service aims to assist overseas companies in registering their overseas-manufactured goods with the TGA of Australia and obtaining approval for sale within Australia. Led by seasoned regulatory registration experts with over 25 years of experience, we are well-versed in the registration regulations and requirements of the Australian TGA. Our expertise enables us to assist your company in efficiently completing the overseas product registration process in Australia and provide comprehensive support for the future sales and market expansion of your product in Australia.
Our overseas product registration services, including services of medical device with or without CE Mark, in Australia encompass the following:
- Consultation and assessment
- Preparation of registration documentation
- Registration application
- Communication, coordination, and representation services