Design History Files (DHF), Device Master Records (DMR), and Device History Records (DHR) are key building blocks used in the design, development, manufacturing, and cGMP compliance for the Medical Device Industry.
Design History File (DHF), the Device Master Record (DMR) and the Device History Record (DHR) – Principles on Lean Documents and Lean Configuration - Webinar By GlobalCompliancePanel
13 December 2011, Wilmington, United States
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online training webinars
online training webinars, 1000 N West Street, DE, Suite 1200, Wilmington, 19801, United States
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Global compliance panel
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