Introduction

This webinar is focused on understanding the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification on commercializing products.

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• Further event details More information about the event

Venue

Online Training

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

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• Venue information More information about the venue

Organised by

GlobalCompliancePanel

Contact information

Mr webinars web
Online Training, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
Contact us by email

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