Concordia Medical’s Quality Management System

Concordia Medical is committed to supporting our partners through design, development, and manufacturing.  Our ISO 13485:2003 certified and FDA QSR compliant Quality Management System is able to support all aspects of medical device design and manufacturing.

Whether the need is Design Control documentation to support regulatory submissions, Risk Management, or fully validated manufacturing processes, Concordia has the expertise to serve as a committed partner in the commercialization of new and innovative medical devices.

Concordia Medical Quality Policy

“Concordia Medical consistently provides high quality products and services that meet or exceed customer expectations, as well as conform to applicable regulatory requirements.”


Click above image to ISO 13485:2003 Certificate