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Report for 2017 on the results from the monitoring of veterinary medicinal product residues and other substances in live animals and animal products

机译:2017年关于活体动物和动物产品中兽药残留和其他物质监测结果的报告

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The report summarises the monitoring data collected in 2017 on the presence of residues of veterinary medicinal products and certain substances in live animals and animal products in the European Union. A total of 708,880 samples were reported to the European Commission by the 28 EU Member States. They consisted of 360,293 targeted samples and 55,088 suspect samples reported under Council Directive 96/23/EC, and of 16,542 samples collected at import and 276,957 samples collected in the framework of programmes developed under the national legislation. The majority of Member States fulfilled the minimum requirements for sampling frequency laid down in Council Directive 96/23/EC and in Commission Decision 97/747/EC. Overall in 2017, the percentage of non‐compliant targeted samples (0.35%) was comparable to the previous 10 years (0.25%–0.37%).
机译:该报告总结了2017年收集的有关欧盟中活兽药和动物产品中兽药残留和某些物质残留的监测数据。 28个欧盟成员国共向欧盟委员会报告了708,880个样品。它们包括根据理事会指令96/23 / EC报告的360,293份目标样本和55,088份可疑样本,以及在进口时收集的16,542份样本和在根据国家立法制定的计划框架下收集的276,957份样本。大多数会员国满足理事会指令96/23 / EC和委员会决定97/747 / EC中规定的最低采样频率要求。总体而言,2017年,不符合要求的目标样本的百分比(0.35%)与之前的十年(0.25%–0.37%)相若。

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