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. Too often, these are cluttered, confusing, and cause many errors due to the way they are created, organized, and managed.
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
31 July 2012, Wilmington, United States
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Online Training, 1000 N West Street, Delaware, Suite 1200, Wilmington, 19801, United States
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