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Samples in periodicals archive:
The PTC Product Development System enables Stryker Navigation to optimize the regulatory compliance process by establishing a common product data management platform for mechanical, electronic and software design with integral processes for automated Design History File (DHF)- and Device Master Record (DMR)-reporting, digital signature procedures, approval workflows and audit reports.
With the PTC Medical Device Template, customers are able to take advantage of the following benefits: --Reporting functionality meeting the demands of audit requests --Data collection support critical to design and delivery: Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) --Process control with workflow for Corrective and Preventative Action (CAPA) "With this offering, PTC is providing a focused service offering for medical device manufacturers to enable them to take advantage of Windchill as a world-class Product Development System while at the same time meeting US FDA requirements.
The MatrixOne PLM platform will help ev3 automate many manual, paper-based processes including the management of device master records (DMR), which contain records of a product's Bill of Materials, components, drawings, labels and other documentation.