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.
Implementing a Quality Management System for Medical Devices and In Vitro Diagnostics
30 May 2014, michigan., United States
Introduction
Venue
online
online, 201,N Squirrel road,, Auburn Hills,, Suite 1007,, michigan., 48326., United States
Useful links
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
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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