Device Master File
Revision as of 07:19, 25 August 2020 by Dirkjan (talk | contribs) (Created page with "In the FDA Regulations a '''Device Master File''' (DMF) means a compilation of records describing the design history of a finished device. Compare Devi...")
In the FDA Regulations a Device Master File (DMF) means a compilation of records describing the design history of a finished device.
Compare Device Master Record