The EU legislation on CE-marking: Medical devices document will guide you through the whole process of CE-marking. The directive has been modified and will enter into force not later than March 21 2010. 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.
