Sep 20, 2023
We are the pioneer in providing CE Marking and Certification regulatorly solution in Europe. Get Clinical Evalution for your Medical Devices
Australia has implemented a new regulatory framework for CE mark for medical devices, moving away from the CE marking system used in Europe. The Therapeutic Goods Administration (TGA) in Australia is responsible for regulating medical devices. It's essential to note that regulations and requirements can change over time. I recommend checking the latest information on the TGA website or consulting with our regulatory expert to ensure compliance with current regulations regarding medical devices in Australia
