In this Cognitio episode, host Tim Boyle is joined by Adele Barnard to explore the fast-changing world of implantable medical device regulation in Australia. Drawing on Adele’s first-hand industry experience, the episode unpacks the TGA’s definition of medical devices, the full lifecycle from pre-approval to post-market surveillance, and the critical steps that sponsors and manufacturers must navigate. Listeners will hear real-world case studies — from multimillion-dollar penalties to high-profile media scrutiny — that have shaped recent reforms. We look at how global alignment, stronger clinical evidence requirements, and robust registry data are redefining compliance, patient safety, and market access. Whether you’re in regulatory affairs, product development, or executive leadership, this is essential listening for staying ahead in the evolving MedTech regulatory landscape.

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