Introduction

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.

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Venue

online training webinars

online training webinars, 1000 N West Street, DE, Suite 1200, Wilmington, 19801, United States

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Organised by

Global compliance panel