D
daamor
I'm looking for a comparison matrix of QMS elements from ISO13485/21 CFR 820 VS. ICH Q10 (new guidance on QMS for pharma).
From a practical standpoint- I'm trying to expand my knowledge base to be able to do a QMS audit on pharma companies. Most of the work I've done is in med devices.
Does anybody know where I can get good comparison on differences between QMS elements and common deliverables (V&V, etc.) in pharma vs. med dev?
From a practical standpoint- I'm trying to expand my knowledge base to be able to do a QMS audit on pharma companies. Most of the work I've done is in med devices.
Does anybody know where I can get good comparison on differences between QMS elements and common deliverables (V&V, etc.) in pharma vs. med dev?
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