This episode provides a comprehensive overview of Australia's medical device regulations, governed by the Therapeutic Goods Administration (TGA). We explore the Therapeutic Goods (Medical Devices) Regulations 2002, detailing the risk-based classification system, the mandatory Essential Principles for safety and performance, the conformity assessment process, and the critical role of the Australian Register of Therapeutic Goods (ARTG) for market entry. Key Questions: • What is the TGA and what is its role in regulating medical devices in Australia? • How does the Therapeutic Goods (Medical Devices) Regulations 2002 impact market entry? • What are the different risk classifications for medical devices and why do they matter? • What are the 'Essential Principles' that every device must meet for TGA approval? • How do conformity assessment procedures differ for low-risk versus high-risk devices? • What is the ARTG and why is it critical for selling your device in Australia? • What are a manufacturer's post-market responsibilities after a device is approved? Ready to turn these insights into your competitive edge? Pure Global’s regulatory experts guide MedTech companies through every step of 30+ markets worldwide. Explore how we can accelerate your market entry at https://pureglobal.com or email [email protected] for tailored support.