Albright Technologies maintains an ISO 13485:2016 Quality Management System for medical devices, which includes the ISO 9001 standard and additional medical device specific requirements. The company’s ISO 13485:2016 Quality Management System is certified by TÜV SÜD America Inc. based in Peabody, Massachusetts. This allows us to mold all forms of medical devices, including short term implants and lifelong implants, while meeting regulatory requirements.
Albright has established quality initiatives to ensure compliance with federal guidelines. Our employees are trained, experienced, dedicated and committed to delivering outstanding customer value by providing rapidly produced silicone products and services that meet or exceed our customers’ requirements at all times.
One of our main goals as an enterprise is to continuously improve our products, services, processes and business relationships.
We mold high quality parts with extremely short lead times in order to meet our customer’s needs and regulatory requirements. We do this by developing new technology for molding polymers, continually improving our business practices and maintaining an Effective Quality Management System.
Along with our high quality products and standards, Albright Technologies is committed to making sure our quality requirements and specifications are not only met, but exceeded. With an ITAR registration we are able to bring significant design and manufacturing capabilities to a broader customer base and positions us to further demonstrate our commitment to and understanding of government market segments. Click here to learn more about our ITAR registration.