根据欧盟条例（EC No 396/2005?章的规定，UPL Europe Ltd. 提交了该修订申请。目前敌菜宁在块根芹中现有的最大残留限量为0.01mg/kg，拟议的最大残留限量为0.15mg/kg（需要进一步的风险管理考虑）、/div>
部分原文报道如下９/div>
In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant UPL Europe Ltd. submitted an application to the competent natio
nal authority in Germany (e
valuating Member State, EMS) to raise the existing maximum residue level (MRL) to 0.15 mg/kg for the active substance phenmedipham in celeriac. The submitted residue trials are sufficient to derive a tentative MRL of 0.15 mg/kg, pending further investigation of nature of phenmedipham residues in root crops. For this assessment EFSA co
nsidered that the available sugar beet me
tabolism data can be extrapolated to celeriac on a tentative basis. The acceptability of such proposal shall be further co
nsidered by risk managers. Adequate analytical methods for enforcement are available to co
ntrol the residues of phenmedipham in celeriac at the validated limit of quantification (LOQ) of 0.01 mg/kg. Since the current MRL application was submitted before the finalisation of the EU pesticides peer review of the renewal of the approval of phenmedipham, the co
nsumer exposure assessment was performed according to the co
nclusions on the toxicity of phenmedipham from the first approval under Directive 91/414/EEC. Accordingly, the long‐term intake of residues of phenmedipham resulting from the existing and the intended uses does not indicate a risk to co
nsumer health. The present assessment does not co
nsider the data gaps identified in the co
ntext of the renewal of the approval of phenmedipham under Regulation (EC) No 1107/2009 which prevented experts to derive toxicological reference values (TRVs) for phenmedipham, to derive the risk assessment residue definition for root crops other than sugar beet and to co
nclude on the toxicity of relevant me
tabolites.
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