ArticleEFSA journal. European Food Safety Authority2025
Modification of the existing maximum residue levels and setting of import tolerances for trifloxystrobin in various crops.
Article in EFSA journal. European Food Safety Authority, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
- Prediction of human exposure and first-pass metabolism of the fungicide trifloxystrobin using an in vitro intestinal pancreatin and Caco-2/HT29-MTX model.Archives of toxicology · 2026Article
- Modification of the existing maximum residue levels and setting of import tolerances for trifloxystrobin in various crops.EFSA journal. European Food Safety Authority · 2025Article
Corrections and comments
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Authors and funding
22 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In accordance with Article 6 of Regulation (EC) No 396/2005, the applicant Bayer AG Crop Science Division submitted a request to the competent national authority in the Netherlands to modify the existing maximum residue levels (MRLs) for trifloxystrobin in table olives, olives for oil production, celeries, globe artichokes, leeks, herbal infusions from flowers, leaves and herbs and seed spices. In addition, a request was submitted to set an import tolerance in linseeds based on authorised use of trifloxystrobin in Canada. The data submitted in support of the request were found to be sufficient to derive MRL proposals for all the crops under assessment except for herbal infusion from flowers, leaves and herbs. Adequate analytical methods for enforcement are available to control the residues of trifloxystrobin on the commodities under consideration at the validated limit of quantification (LOQ) of 0.01 mg/kg. Based on the risk assessment results, European Food Safety Authority (EFSA) concluded that the short-term and long-term intake of residues resulting from the use of trifloxystrobin according to the reported agricultural practices is unlikely to present a risk to consumer health. The consumer risk assessment shall be regarded as indicative and affected by uncertainties.
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Registered trials
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