Samuel Linton

Chris is an extremely knowledgeable expert with a wealth of experience dealing with RA / QA issues at FDA regulated companies.

Chris is an extremely knowledgeable expert with a wealth of experience dealing with RA / QA issues at FDA regulated companies. AT AI he was an invaluable resource in helping us to ensure regulatory compliance without sacrificing our efficiency.

Samuel LintonDirector of Operations, Integrated SolutionsPromega






About Christopher Ford

Christopher Ford is an expert in global medical device manufacturing compliance with over 20 years of experience, specializing in Class II and Class III medical devices and combination products. He is a certified ISO 13485 Lead Auditor, with over 600 audits under his belt, and he works with organizations of all sizes. His approach to compliance requirements balances customer needs with business objectives, while assuring that all regulatory requirements are met.