With over 23 years of experience in the medical device industry and as a qualified Lead Auditor Practitioner in BS EN ISO 13485, I am dedicated to helping organisations navigate the complexities of compliance, testing, and patient safety. Through consultancy, I provide expert guidance to ensure medical devices meet the highest standards of quality and regulatory expectations, including audit readiness, clinical evaluation (CER/CEP), and Post‑Market Surveillance (PMS) support.

​

I believe that strong Quality and Regulatory frameworks are essential to ensuring devices are thoroughly tested and safe for patient use. This also extends to the safe handling and decontamination of reusable medical devices, ensuring protection for the user, the reprocessor, and ultimately the patient.

My commitment to this field drives me to stay current with evolving standards, regulations, and best practices. I am always seeking to expand my skills and knowledge to enhance the services I offer and to better support organisations in delivering safe and compliant medical technologies.

​

When you work with me, you can expect an honest, open, and knowledgeable partner who will guide you through the ever‑changing landscape of medical device regulations. My goal is simple: to help you succeed in developing and delivering high‑quality, safe medical devices to the healthcare market.