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Veris Manufacturing receives ISO 13485 recertification with zero nonconformances found

February 2016 – Upon completion of an external audit of Veris’ compliance with international quality standards, Veris Manufacturing achieved recertification of international standard ISO 13485 without a single nonconformance. ISO 13485 is the current international standard for medical device and component manufacturers in implementation of a system for quality management. Compliance with this standard ensures a commitment to meeting customers’ needs for quality products.

This audit was conducted by Independent International Organization for Certification (IIOC) member ABS Quality Evaluations who provide quality assessment across the globe. Maintaining this certification requires that a company be evaluated every three years for compliance in quality management such as record controls, internal auditing procedures, and preventative actions. Given this, accomplishing zero nonconformances indicates no faults in compliance with the standard, as well as a strict dedication to quality of both product and service to customers.

For more information please contact us at Verismfg.com, or Facebook.com/VerisMfg

http://www.abs-qe.com/management-systems-certification.html
http://www.abs-qe.com/medical-management-systems.html
http://www.emergogroup.com/resources/articles/what-is-iso-13485-certification
http://www.iso13485.com/common-questions-iso13485
http://www.nqa.com/Nqa.com/media/.../ISO-13485-Registration-Guidance.pdf

 

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