Vanguard EMS Completes cGMP/QSR Compliance, FDA Registration

BEAVERTON, OR February 25, 2013 – Vanguard EMS announced today that it has successfully completed the audit for cGMP/QSR compliance and FDA registration as a medical device contract manufacturer.  This accomplishment demonstrates Vanguard’s commitment to excellence in quality systems and management control, including traceability, process validation, and corrective and preventative action.

Vanguard manufactures infant respirators, surgical ultrasound drug delivery systems, and other complex electro-mechanical finished devices.

“This is a logical next step in our services to medical device companies,” says Floyd Sutz, CEO.  “We look forward to expanding our service offering in this area to more customers.”

About Vanguard EMS
Vanguard EMS serves market leading companies in medical, defense and industrial markets. Vanguard provides dedicated customer focused teams combined with operational excellence. Vanguard is ISO 9001, ISO 13485, FDA Registered, AS9100 and ITAR certified. Vanguard’s 70,000 square foot facility in Beaverton, Oregon offers prototype services, state-of-the-art SMT lines, in-circuit test, full functional test, and complete system build capability. The company has been in business for 25 years.

Contact:
Sara Carlson
503-672-4240
sara.carlson@vanguard-ems.com

2016-03-16T14:47:24+00:00