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European veterinary regulations - post-Prague evaluation

European member states were required to transpose new EU medicines legislation, including Directive 2004/28 EC amending Directive 2001/82 EC on veterinary medicinal products, into national law by the end of last October. Informa Life Sciences' 3rd annual conference on the Regulation of Veterinary Medicines in Europe in Prague, Czech Republic, last month, highlights that six months on, this has been done with varied degrees of success in the different states. Beata Fojcik examines two very different countries - Hungary, a new accession member state - and Norway, which is not part of the EU - to see how they have dealt with the new legislation.

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