EU legislation on CE-marking: In vitro diagnostic medical devices
|
The EU legislation on CE-marking: In vitro diagnostics medical devices document will guide you through the whole process of CE-marking. The directive has been revised only. In the document you will be first provided with an explanation on the EU directive concerned. Secondly, information is given on how to apply the legislative demands in only nine steps. The document is also based on the experiences of CBI while assisting exporters in developing countries. See the related instruction document for a general overview on CE marking implementation.
Download EU legislation on CE-marking: In vitro diagnostic medical devices
|
 |
Pages: 12 Size: 203 Kb Download time: 4 Sec (at 56k6)
|
EU Member State legislation
| Member States overview: Implementation of EU legislation on CE marking of in vitro diagnostic medical devices |
Relevant Market Sectors
search again
Search by category
OR
Search by keyword
Related Documents
- EU legislation on CE-marking: Instruction on implementing CE-marking
- Norway legislation on CE Marking: In vitro diagnostic medical devices
- EU legislation on CE-marking: Medical devices
- EU legislation on CE-marking: Active implantable medical devices
- EU legislation on CE-marking: Medical devices (case)
External Links
Questions?
On market access requirements: marketaccess@cbi.eu
On CBI market information: marketinfo@cbi.eu
