Christopher Ford was brought into R2 as an expert in Quality Control and Compliance. During his time at R2 Christopher was instrumental in revamping our Quality Policy and identifying and recommending changes to problem areas. He oversaw the implementation of change and was the contact point for our interface with state and federal auditors. I would highly recommend Christopher.
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.
