Corvalent gets the rubber stamp approval and fully meets the requirements of ISO13485:2003 re-certification without a single non-conformance

Austin, TX, October 29, 2014 – Corvalent announced today that once again it has achieved a major milestone by receiving ISO13485-2003 re-certification.  ISO 13485-2003 is an international ISO standard that defines the requirements for a comprehensive management system for the design and manufacture of medical devices.   Ana Rudloff, Quality Assurance & Doc Control Specialist stated, […]