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.
Live webinar on Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs By compliance2go
4 June 2012, Houston, Texas, United States
Introduction
Venue
Online
Online, 10777 Westheimer Suite 1100, Houston, Texas, 77042, United States
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Organised by
Compliance2go
Contact information
Miss Trisha Paul
10777 Westheimer Suite 1100, Houston, Texas, 77042, United States of America
1.877.782.4696
Contact us by email
10777 Westheimer Suite 1100, Houston, Texas, 77042, United States of America
1.877.782.4696
Contact us by email
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