I am the co-founder of Pure Global, a medical device regulatory consulting firm helping MedTech manufacturers secure international regulatory approvals and expand into new markets. With more than 20 years of experience in software engineering and over 15 years in finance, I bring a multidisciplinary perspective to the medical device industry, combining technical expertise, regulatory strategy, data intelligence, and commercial insight. At Pure Global, I help manufacturers navigate complex regulatory pathways across the United States, European Union, Middle East, Canada, Latin America, Asia, and Australia. My work focuses on using AI-native, data-driven regulatory intelligence to identify practical compliance pathways, monitor global regulatory changes, and accelerate market access whil...