Difference between revisions of "CE Marking Courses"
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[[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 | |||
Who should attend | * Those who need in-depth knowledge of medical devices directives | ||
Those working in regulatory, design, development, manufacturing or marketing roles | * Organisations preparing own branding or private labelling. | ||
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.