With over 22 years of experience in the medical device industry and as a qualified Lead Auditor in BS EN ISO 13485, I am passionate about helping others navigate the complexities of the medical devices industry, testing, compliance, and patient safety. Through consultancy, I provide expert guidance to ensure that medical devices meet the highest standards of quality and regulatory compliance.

I firmly believe that robust Quality and Regulatory processes are essential for ensuring medical devices are properly tested and safe for patient use. This extends to the safe handling and decontamination of reusable medical devices, protecting not only the repressor and user but also the patient.

 

My dedication to this field drives me to stay up to date with the latest standards, regulations, and industry best practices. I thrive on collaborating with like-minded professionals who share my commitment to excellence in healthcare innovation.

When you work with me, you can expect an honest, open, and knowledgeable partner who is committed to ensuring compliance and guiding you through the evolving landscape of medical device regulations. My goal is to help you succeed in bringing safe, high-quality medical devices to the ever-growing healthcare industry.