Difference between revisions of "CE Marking Courses"

Jump to navigation Jump to search
175 bytes added ,  08:27, 5 February 2013
no edit summary
(Created page with "Category:Courses, Training{{Knoppen}} <noinclude><!------------------------------------------------ * READ THIS FIRST * Only edit this page if you can improve the content....")
 
Line 1: Line 1:
[[Category:Courses, Training]]{{Knoppen}}
[[Category:Courses, Training]]{{Knoppen}}
<noinclude><!------------------------------------------------ 
 
* READ THIS FIRST
The aim of the training is to enable delegates to develop a detailed understanding of the key European Directives, in particular the Machinery Directive, in relation to CE Marking.
* Only edit this page if you can improve the content.  
This training on CE Marking will provide a detailed
* Improper use of this page will lead to permanent banning.
 
* Please do not edit the sponsored link on the top right corner.
review of the requirements of the main directives in
* Please start editing this page after the /noinclude 
 
* -------------------------------------------------></noinclude>
relation to CE Marking and explains in detail the process
This page is still empty. If you know something about this product, please share your knowledge with others.
 
required to CE Mark a machine.
 
 
Who should attend?
Those working in regulatory, design, development, manufacturing or marketing roles
Internal auditors or those planning to become internal auditors
Those who need in-depth knowledge of medical devices directives
Organisations preparing own branding or private labelling.

Navigation menu