Anastassiadou Maria, Bernasconi Giovanni, Brancato Alba, Carrasco Cabrera Luis, Ferreira Lucien, Greco Luna, Jarrah Samira, Kazocina Aija, Leuschner Renata, Magrans Jose Oriol, Miron Ileana, Nave Stefanie, Pedersen Ragnor, Reich Hermine, Rojas Alejandro, Sacchi Angela, Santos Miguel, Scarlato Alessia Pia, Theobald Anne, Vagenende Benedicte, Verani Alessia
EFSA J. 2021 Jan 22;19(1):e06389. doi: 10.2903/j.efsa.2021.6389. eCollection 2021 Jan.
In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Corteva submitted a request to the competent national authority in Finland to modify the existing maximum residue levels (MRLs) for the active substance clopyralid in various commodities. The data submitted in support of the request were found to be sufficient to derive MRL proposals for wheat, oat and for animal commodities. An adequate analytical method for enforcement is available to control the residues of clopyralid in the plant commodities under consideration at the validated limit of quantification (LOQ) of 0.01 mg/kg. The analytical methods for animal commodities are validated at LOQ of 0.01 mg/kg, but demonstration of extraction efficiency is lacking. Based on the risk assessment results, EFSA concluded that the short-term and long-term intake of residues resulting from the use of clopyralid according to the reported agricultural practices is unlikely to present a risk to consumer health provided that risk mitigation measures are in place to avoid clopyralid residues in rotational and/or succeeding crops.
根据欧盟法规(EC)No 396/2005第6条,申请人科迪华(Corteva)向芬兰国家主管当局提交了一项请求,要求修改活性物质氯吡脲在各种商品中的现有最大残留限量(MRLs)。所提交的支持该请求的数据被认为足以得出小麦、燕麦和动物商品的MRL建议。有合适的执法分析方法可用于在0.01 mg/kg的验证定量限(LOQ)下控制所考虑的植物商品中氯吡脲的残留。动物商品的分析方法在0.01 mg/kg的LOQ下得到验证,但缺乏提取效率的证明。基于风险评估结果,欧洲食品安全局(EFSA)得出结论,只要采取风险缓解措施以避免氯吡脲残留在轮作和/或后续作物中,按照报告的农业实践使用氯吡脲所产生的残留短期和长期摄入对消费者健康不太可能构成风险。