Introduction

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. The course covers all relevant topics in brief associated with the Directives and Guidance Documents, the reasons behind their introduction and a review of methods for effective implementation

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• Further event details More information about the event

Venue

Compliance2go Webinar

Online, Compliance2go Webinar, 10777 Westheimer Suite 1100, Houston, Texas, Houston, 77043, United States

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• Venue information More information about the venue

Organised by

Compliance2go

Contact information

Mr Admin
10777 Westheimer Suite 1100, 10777 Westheimer Suite 1100, Houston, United States of America
8777824696
Contact us by email

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