Difference between revisions of "CE Marking Courses"
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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. | |||
This training 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. | |||
Revision as of 08:27, 5 February 2013
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.
This training 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.