Terri Ross

Christopher is a disciplined and experienced QA/RA professional who led our team in the development of SOPs, CAPA handling, updated training, and ISO audit preparation.

Christopher is a disciplined and experienced QA/RA professional who led our team in the development of SOPs, CAPA handling, updated training, and ISO audit preparation. I have great respect for his dedication, determination, extensive knowledge and strong sense of ethics. He was invaluable in the preparation for and handling of FDA and state audits. He is an articulate, versatile and creative professional. I am happy to recommend him without reservation.

Terri RossCommodities ManagerCoolSystems, Inc






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.