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Implementing a Quality Management System for Medical Devices and In Vitro Diagnostics

30 May 2014, michigan., United States


Introduction
This webinar is intended to help you get familiar with US quality system regulations and how to implement an FDA-compliant quality management system for medical devices including in vitro diagnostic medical devices (IVDs). Device manufacturers are required to establish and maintain the FDA-compliant quality management systems, where appropriate and applicable, including design control.
Venue
online

online, 201,N Squirrel road,, Auburn Hills,, Suite 1007,, michigan., 48326., United States

Organised by
Global Compliance Trainings
Contact information
Mr john gordan
201,N Squirrel road, Suite 1007, Auburn Hills, Suite 1007,, Auburn Hills,, michigan., 48326., United States of America
2482120588
Contact us by email

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