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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• Further event details More information about the event

Venue

Online Training Webinars

Online Training Webinars, 1000 N West Street | Suite 1200, Wilmington, 19801, United States

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• Venue information More information about the venue

Organised by

GlobalCompliancePanel

Contact information

Mr David Ross
Wilmington, 19801, United States of America
800-447-9407
Contact us by email

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