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QMS Auditing
Our auditors are certified by the American Society for Quality and we are experienced in performing first, second and third party audits to ensure compliance with general industrial ISO 9000 requirements as well as more stringent ISO 13485 and FDA 21 CFR 820 requirements for the Medical Device Industry.
We have experience in performing internal system, process, and product level audits as well as performing supplier audits and have successfully lead multiple companies through the successful registrar and governmental audits.
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