Heidi Naderi brings a decade of specialised, hands-on experience in medical device regulation, with a focus on the EU, UK, and Middle East markets. Her expertise uniquely combines international experience as a medical device regulator, compliance adviser, and lecturer in regulatory compliance and assessments.Heidi's deep knowledge spans the rapidly evolving regulatory frameworks, including the UK’s medical device regulations, the EU’s Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR), and the Saudi Food and Drug Authority’s (SFDA) Medical Devices Marketing Authorization (MDMA) requirements. She has successfully led and supported numerous international medical device companies, guiding them from initial concept through to full market readiness. Her hands-on approach has been instrumental in ensuring the successful launch of multiple medical devices across diverse markets.