Difference between revisions of "CE Marking Courses"
Jump to navigation
Jump to search
(Created page with "Category:Courses, Training{{Knoppen}} <noinclude><!------------------------------------------------ * READ THIS FIRST * Only edit this page if you can improve the content....") |
|||
| (One intermediate revision by the same user not shown) | |||
| Line 1: | Line 1: | ||
[[Category:Courses, Training]]{{Knoppen}} | [[Category:Courses, Training]]{{Knoppen}} | ||
[[File:Ce logo.gif|thumb|right|CE logo]] | |||
The aim of '''CE Marking Course''' is to enable delegates to develop a detailed understanding of the key European Directives, in particular the Machinery Directive, in relation to CE marking. | |||
This course on CE Marking will provide a detailed review of the requirements of the main directives in relation to CE Marking and explains in detail the process 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. | |||
Latest revision as of 10:32, 5 February 2013
The aim of CE Marking Course is to enable delegates to develop a detailed understanding of the key European Directives, in particular the Machinery Directive, in relation to CE marking. This course on CE Marking will provide a detailed review of the requirements of the main directives in relation to CE Marking and explains in detail the process 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.