Currently browsing "DMR"
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From Compliance to Competitive Advantage: Rethinking the Device Master Record in the Digital Era
The New Face of Quality in MedTech In medical device manufacturing, documentation is destiny. Among every procedure, drawing, and record, the Device Master Record (DMR) stands apart as the canonical blueprint that translates design intent into a reliable, repeatable, and auditable reality. For years, organizations treated the DMR as a static binder compiled only because […]
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Exploring the DMR Framework in Quality Systems
The Device Master Record (DMR) is a critical component of quality systems, particularly in industries like medical devices, pharmaceuticals, and manufacturing. It is a foundational document encompassing all the essential information required to manufacture a device. A well-organized DMR ensures compliance with regulatory standards and safeguards product quality and safety. This article delves into the […]
