From Compliance to Competitive Advantage: Rethinking the Device Master Record in the Digital Era
23 min read
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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