With ten years of experience in the medical device industry, Sarah has built a wide breadth and depth of knowledge across multiple disciplines spanning regulatory, design and development, quality assurance, process validation and data security compliance. 

Sarah is passionate about promoting innovation in medical devices, combining commercial insight, pragmatism, and solution-oriented approaches to help clients gain regulatory approval for their medical devices. 

Sarah’s area of expertise is software as a medical device (SaMD), including AI/ML. She has also worked in quality and regulatory roles in the wound care and disinfection markets.

Her hobbies and interests include reading, up-cycling of furniture and walking.