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ISO 13485 Audit Success! Re-certified!

ISO 13485 Audit Success! Re-certified!

March 2019 – Veris recently went through the ISO 13485:2016 audit and came out with flying colors! During this audit Veris Manufacturing achieved re-certification. ISO 13485:2016 is the current international standard for medical devices and component manufacturers. Maintaining this certification requires that a company be evaluated every year for compliance in quality management such as record controls, internal auditing procedures, and preventative actions. ISO 13485:2016 is designed to respond to latest quality management system practices, including changes in technology and regulatory requirements and expectations.

If your company requires a copy of any of our certificates, please email us. We are happy to provide them to you.

 

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