Targeted review of maximum residue levels (MRLs) for dicofol.
MRL setting
consumer risk assessment
dicofol
non‐approved active substance
residue definitions
toxicological evaluation
Journal
EFSA journal. European Food Safety Authority
ISSN: 1831-4732
Titre abrégé: EFSA J
Pays: United States
ID NLM: 101642076
Informations de publication
Date de publication:
Nov 2023
Nov 2023
Historique:
medline:
29
11
2023
pubmed:
29
11
2023
entrez:
29
11
2023
Statut:
epublish
Résumé
In accordance with Article 43 of Regulation (EC) 396/2005, EFSA received a request from the European Commission to review the existing maximum residue levels (MRLs) for the non-approved active substance dicofol in view of the possible lowering of the MRL. EFSA investigated the origin of the current EU MRLs. All existing EU MRLs reflect previously authorised uses in the EU or are based on obsolete Codex Maximum Residue Limits. Furthermore, in view of the limitations of the toxicological dataset and related uncertainties, the existing toxicological reference values derived at the EU level cannot be confirmed for dicofol. EFSA therefore proposed lowering all existing EU MRLs for dicofol to the limit of quantification.
Identifiants
pubmed: 38027437
doi: 10.2903/j.efsa.2023.8425
pii: EFS28425
pmc: PMC10664694
doi:
Types de publication
Journal Article
Langues
eng
Pagination
e08425Informations de copyright
© 2023 European Food Safety Authority. EFSA Journal published by Wiley‐VCH GmbH on behalf of European Food Safety Authority.
Déclaration de conflit d'intérêts
If you wish to access the declaration of interests of any expert contributing to an EFSA scientific assessment, please contact interestmanagement@efsa.europa.eu.
Références
EFSA J. 2017 Jul 25;15(7):e04929
pubmed: 32625585
EFSA J. 2018 Jan 15;16(1):e05147
pubmed: 32625691
EFSA J. 2018 Jun 07;16(6):e05311
pubmed: 32625944
EFSA J. 2023 Jul 24;21(7):e08113
pubmed: 37492499