Device Master Record
Revision as of 07:19, 25 August 2020 by Dirkjan (talk | contribs) (Created page with "In the FDA Regulations a '''Device Master Record''' (DMS) means a compilation of records containing the prodedures and specifications for a finishe...")
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
Note: 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???
