Dirkjan: 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..."

2020-08-25T07:19:26Z

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..."

New page

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

Compare [[Device Master File|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???
[[Category:fda]]

[[Category:CFR]]

[[Category:CFR 21-820.40]]

[[Category:Document Controls]]

[[Category:FDA]]

[[Category:Quality System Requirements]]

[[Category:Term]]

Device Master Record - Revision history

Dirkjan: 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..."