2023年5月5日，歐盟食品安全局（EFSA）發(fā)布消息稱，擬修訂綠草定（triclopyr）在動物產(chǎn)品中的最大殘留限量。
根據(jù)歐盟條例（EC）No 396/2005第6章的規(guī)定，Corteva Agriscience International Sàrl提交了該修訂申請。經(jīng)過評估，歐盟食品安全局得出結(jié)論，根據(jù)所報道的農(nóng)業(yè)實踐，短期和長期攝入因使用綠草定而產(chǎn)生的殘留物不太可能對消費者健康構(gòu)成風(fēng)險。在提交MRL審查所要求的確認數(shù)據(jù)之前，消費者風(fēng)險評估是指示性的。部分原文報道如下：
In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Corteva Agriscience International Sàrl submitted a request to the competent national authority in the Netherlands to modify the existing maximum residue levels (MRLs) for the active substance triclopyr in animal commodities. The data submitted in support the request were found to be sufficient to derive MRL proposals for swine and ruminant edible commodities and for ruminant milks considering residue levels expected for the intended uses on grassland. Adequate analytical methods for enforcement are available to control the residues of triclopyr on the commodities under consideration at the validated limit of analytical quantification (LOQ) of 0.01 mg/kg. based on the risk assessment results, EFSA concluded that the short-term and long-term intake of residues resulting from the uses of triclopyr according to the reported agricultural practices and the derived MRLs in products of animal origin is unlikely to present a risk to consumer health. The consumer risk assessment is indicative pending the submission of the confirmatory data requested under the MRL review.
根據(jù)歐盟條例（EC）No 396/2005第6章的規(guī)定，Corteva Agriscience International Sàrl提交了該修訂申請。經(jīng)過評估，歐盟食品安全局得出結(jié)論，根據(jù)所報道的農(nóng)業(yè)實踐，短期和長期攝入因使用綠草定而產(chǎn)生的殘留物不太可能對消費者健康構(gòu)成風(fēng)險。在提交MRL審查所要求的確認數(shù)據(jù)之前，消費者風(fēng)險評估是指示性的。部分原文報道如下：
In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Corteva Agriscience International Sàrl submitted a request to the competent national authority in the Netherlands to modify the existing maximum residue levels (MRLs) for the active substance triclopyr in animal commodities. The data submitted in support the request were found to be sufficient to derive MRL proposals for swine and ruminant edible commodities and for ruminant milks considering residue levels expected for the intended uses on grassland. Adequate analytical methods for enforcement are available to control the residues of triclopyr on the commodities under consideration at the validated limit of analytical quantification (LOQ) of 0.01 mg/kg. based on the risk assessment results, EFSA concluded that the short-term and long-term intake of residues resulting from the uses of triclopyr according to the reported agricultural practices and the derived MRLs in products of animal origin is unlikely to present a risk to consumer health. The consumer risk assessment is indicative pending the submission of the confirmatory data requested under the MRL review.
