Albright Technologies Completes ISO 13485:2003 Certification Audit
February 1, 2016
Albright Technologies, Inc. has completed its ISO 13485:2003 re-certification audit, conducted by TUV SUD, and received an extension to its registration through 2018. Albright provides rapid silicone prototype and production molding solutions to the medical device market.
The ISO 13485:2003 standard specifies requirements for a Quality Management System focusing on medical devices. In order to maintain certification, an organization's quality management system must display the ability to provide medical related components that consistently meet customer and regulatory requirements relevant to medical device application standards.
"As we develop and grow, we have continued to refine our ISO 13485:2003 quality management system so that we can confidently provide our medical device customers with the highest quality silicone molded parts," said Matthew Bont, Director of Operations at Albright Technologies.
For more information contact:
Albright Technologies
25 Litchfield Street
Leominster, MA 01453
978-466-5870 / 800-501-6335
www.albright1.com
< back