Device master record template $ 150.00 form/template used to organize and consolidate product information intended to provide the technical documentation details associated with a. The requirement for a device master record is outlined in the fda’s quality system. The model of the dmr table should have a formal index form as. | medical device validation, regulation,. A lot of the documents are not in the device master record, but are referenced in the dmr as to where the document is located (document control office, engineering library,.
