Tom Clarke
Quality & Regulatory Consultant
I have over 15 years’ experience in the medical device industry, having held a range of quality and regulatory roles in that time, including Head of Quality and Regulatory Affairs for a manufacturer of IVD devices . For the past 7 years, I’ve worked independently but began working with Advena in 2023 to support their clients across the medical device, IVD, and wider life sciences sectors.
I’m a qualified lead auditor, specialising in helping clients design and implement quality management systems that are both practical and compliant. I’m a strong believer that there is no one-size-fits-all solution, and I take pride in working closely with each client to build systems that reflect their unique needs and ways of working.
