I came across an FDA guidance document – not entirely recent; however, I found it very interesting and worth sharing. It is on voluntary submissions of audit reports done by auditing bodies outside of the FDA.
[fa icon="clock-o"] 4/5/13 7:11 AM [fa icon="user"] Ryan Kasun [fa icon="folder-open'] Japan PMDA, EU, audits, TGA, GHTF, FDA, health canada, quality improvements, iso 13485
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