Chris has over 15 years of experience in the medical device industry, alongside additional expertise in pharmaceuticals and combination products. He has worked across Manufacturing, R&D, Regulatory Affairs, Compliance, and Quality, giving him a comprehensive understanding of regulated product lifecycles. 

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Most recently, Chris served as Head of Quality, Regulatory, and Compliance at a fast-growing start-up, where he led the successful achievement of ISO 13485 certification and UK MDR compliance. His work enabled the first product approvals in both the UK and US for a complex electronic active device system incorporating software. 

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Chris is committed to keeping patient and user safety at the centre of decision-making. He is known for fostering a strong culture of quality, collaboration, and continuous improvement, bringing teams together to solve challenges and drive sustainable success. 

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