The European Commission has announced a pilot program, to examine the changes that will result form the adoption of the Directive. There are amendments to three Directives: 90/385/EEC relating to active implantable medical devices; 93/42/EEC concerning medical devices; and 98/8/EC concerning the placing of biocidal products on the market. The revised regulatory framework for medical devices is required to be transposed into national law by the 21st of December 2008.
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