Local view for "http://purl.org/linkedpolitics/eu/plenary/2008-06-17-Speech-2-239"
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"en.20080617.35.2-239"2
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As veterinary medicinal products used for the therapeutic treatment and the welfare of animals which are destined for human consumption may give rise to residues of such products in food-producing animals, a risk assessment of the safety limit of residues of all pharmacologically active substances contained in veterinary products needs to be carried out.
The Commission’s proposal to repeal Regulation (EEC) No 2377/90 seeks to resolve the difficulties encountered in the application of the existing legislation. It proposes alternative ways to achieve a high level of consumer protection, coupled with the continued availability and development of veterinary medicinal products for the European market and good functioning of the intra- and extra-Community trade in food of animal origin.
The rapporteur also points out that as the ultimate goal is human health protection, a more consistent approach is required for the risk analysis and control of residues of pharmacologically active substances, which may appear in food produced in or imported into the European Union."@en1
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