##  [Remote Internal Audit of QMS Systems for 21 CFR 820 and ISO 13485:2016 Compliance](/index%2ephp/case-studies/remote-internal-audit-of-qms-systems-for-21-cfr-820-and-iso-134852016-compliance) 

- [Medical Devices](/index%2ephp/case-studies-main-categories/medical-devices)
- [Quality, Compliance, & Audit (QMS)](/index%2ephp/case-studies-main-categories/quality-compliance-audit-qms)





[US FDA](/index%2ephp/case-studies-heath-authority/us-fda)

 

 ![Remote Internal Audit of QMS Systems for 21 CFR 820 and ISO 13485:2016 Compliance]()

A leading US-based medical device manufacturer approached Freyr for QMS audit support for 21 CFR 820 and ISO 13485:2016 compliance. Amidst the current pandemic conditions, Freyr conducted a remote internal QMS audit through a strategic, phase-wise approach, as per the defined regulations in scope, with meticulous planning and by deploying certified auditors.

Download the case study to decipher how Freyr performed on-time and compliant remote internal audits for the QMS systems.



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