Peer review of the pesticide risk assessment for the active substance spiroxamine in light of confirmatory data submitted
In: EFSA journal, Band 19, Heft 2
ISSN: 1831-4732
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In: EFSA journal, Band 19, Heft 2
ISSN: 1831-4732
In: EFSA journal, Band 20, Heft 3
ISSN: 1831-4732
The conclusions of EFSA following the peer review of the initial efficacy assessment and consideration of the effects of water treatment used for the production of drinking water on any residues that might be in raw water carried out by the competent authority of the rapporteur Member State Greece for the pesticide active substances paraffin oils (CAS 64742‐46‐7, 72623‐86‐0 and 97862‐82‐3) are reported. The context of the peer review was that required by Regulation (EC) No 1107/2009 of the European Parliament and of the Council for an amendment in approval conditions. The conclusions were reached on the basis of the evaluation of the efficacy of paraffin oils (CAS 64742‐46‐7, 72623‐86‐0 and 97862‐82‐3) as a fungicide. The reliable endpoints are presented.
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In: EFSA supporting publications, Band 16, Heft 4
ISSN: 2397-8325
According to Regulation (EC) No 396/2005 on maximum residue levels of pesticides in or on food and feed, Member States have to monitor pesticide residue levels in food samples and submit the monitoring results to EFSA and the European Commission. The Standard Sample Description (SSD) is the data model used for reporting the data on analytical measurements of chemical substances occurring in food, feed and water to EFSA. In 2015, EFSA issued a thoroughly revised guidance defining the appropriate SSD codes to describe the samples and the analytical results for the reporting of the 2014 pesticide residues monitoring data. In May 2016, a new guidance was published for the coding of specific SSD data elements for the reporting of the 2015 pesticide monitoring data. In the current document, new coding provisions are delivered for specific data elements to code the data generated in 2016. These provisions take into account the experience of both the previous reporting seasons and the new legislation applicable in 2016. In addition, new explanatory examples on the appropriate coding for specific food samples are provided.
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In: EFSA journal, Band 15, Heft 5
ISSN: 1831-4732
In: EFSA journal, Band 21, Heft 8
ISSN: 1831-4732
In: EFSA journal, Band 17, Heft 6
ISSN: 1831-4732
In: EFSA journal, Band 16, Heft 9
ISSN: 1831-4732
In: EFSA journal, Band 16, Heft 6
ISSN: 1831-4732
In: EFSA journal, Band 16, Heft 5
ISSN: 1831-4732
In: EFSA journal, Band 16, Heft 3
ISSN: 1831-4732
In: EFSA journal, Band 16, Heft 2
ISSN: 1831-4732
According to Article 12 of Regulation (EC) No 396/2005, EFSA has reviewed the maximum residue levels (MRLs) currently established at European level for the pesticide active substance fluquinconazole. Considering the information provided by Member States, neither EU uses nor import tolerances are currently authorised for fluquinconazole within the European Union. Furthermore, no MRLs are established by the Codex Alimentarius Commission (codex maximum residue limits) for this active substance. Therefore, residues of fluquinconazole are not expected to occur in any plant or animal commodity. Nevertheless, available data allowed EFSA to propose a marker residue and limit of quantifications (LOQs) for enforcement against potential illegal uses.
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In accordance with Article 6 of Regulation (EC) No 396/2005, the Australian Government Department of Agriculture and Water Resources submitted two requests to the competent national authority in Denmark to set import tolerances for the active substance haloxyfop‐P in linseed and rapeseed. The data submitted in support of the request were found to be sufficient to derive maximum residue level (MRL) proposals for linseed and rapeseed. Adequate analytical methods for enforcement are available to control the residues of haloxyfop‐P in plant matrices under consideration at the validated limit of quantification (LOQ) of 0.05 mg/kg. EFSA reiterates the recommendation from the Article 12 MRL review that an independent laboratory validation (ILV) should be provided. Based on the risk assessment results, EFSA concluded that the short‐term and long‐term intake of residues resulting from the use of haloxyfop‐P according to the reported agricultural practices is unlikely to present a risk to consumer health.
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