Albright Technologies, Inc., the world’s leader in silicone prototyping and production molding, has completed its ISO 13485:2003 re-certification audit, conducted by TUV SUD and received an extension to its registration through 2018.
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. The extension of this certification proves Albright’s long-term commitment to supply the highest quality silicone components to the medical device marketplace. Albright provides rapid silicone prototype and production molding solutions to the medical device market.
“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. “The successful completion of our ISO 13485 re-certification is recognition for the hard work and commitment of our staff in making Albright Technologies a global leader in silicone molding.”
Albright Technologies, Inc.