Christopher is extremely knowledgeable in the area of medical device regulation, especially documentation requirements and best practices both domestically and abroad. He would be a valuable resource to anyone who deals regularly with FDA or equivalent foreign standards agencies.
About Christopher FordChristopher 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.
