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
Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs By Compliance2go
4 October 2011, Houston, United States
Introduction
Venue
Compliance2go Webinar
Online, Compliance2go Webinar, 10777 Westheimer Suite 1100, Houston, Texas, Houston, 77043, United States
Useful links
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
10777 Westheimer Suite 1100, 10777 Westheimer Suite 1100, Houston, United States of America
8777824696
Contact us by email
Related events
Chemistry Teaching in Practice
9 January 2025 09:30-16:00, Oxford, United Kingdom
TAC 2025 - 60th Anniversary Conference
14 April 2025 09:00 - 16 April 2025 17:00, Guildford, United Kingdom
Top of the Bench Lancashire Local Section Heat
16 January 2025 10:00-15:30, Preston, United Kingdom
Redefining the Chemical Status Quo: Women Catalysts for Equality
11 February 2025 10:00-13:00, Abuja, Nigeria
Search
Advertisement
Spotlight
Explore
Membership
