The European Commission has published an updated list of testing and certification organisations that were notified to test medical devices and diagnostics to the requirements of the EU's Medical Devices Directive and the In Vitro Diagnostics Directive as of September 30 2003. The list is contained in a 414-page volume of the Official Journal of the European Union published on December 12 in Volume 46, C302. It is featured along with the names of all the notified bodies designated by EU member states and the EFTA countries under the new approach directives. The list includes notified bodies from candidate countries as well as designated conformity assessment bodies from third countries with whom the European Commission has concluded a mutual recognition agreement (MRA).
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