In the [[FDA Regulations]] a ''Device Master Record'' ([[DMS]]) means a compilation of records containing the prodedures and specifications for a finished device.

Compare [[Device Master File]]

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Question: The difference between a ''//record//'' and a ''//file//'' is that the record is about the actual device in production and the file is about the actual device during design???
bag
fda_public
created
Fri, 12 Oct 2012 08:21:16 GMT
creator
dirkjan
modified
Fri, 12 Oct 2012 08:21:16 GMT
modifier
dirkjan
tags
CFR
CFR 21-820.40
Document Controls
FDA
Quality System Requirements
Term
creator
dirkjan