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.
Creation of DHFs, DMRs, and DHRs utilizing the principles of Lean Documents and Lean Configuration - Webinar By GlobalCompliancePanel
12 July 2011, Wilmington, United States
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Online Training Webinars, 1000 N West Street | Suite 1200, Wilmington, 19801, United States
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