Targeted review of maximum residue levels (MRLs) for fenpropathrin.
MRL setting
consumer risk assessment
fenpropathrin
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:
Jun 2023
Jun 2023
Historique:
medline:
21
6
2023
pubmed:
21
6
2023
entrez:
21
6
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 fenpropathrin in view of the possible lowering of the MRLs. EFSA investigated the origin of the current EU MRLs. For existing EU MRLs that reflect previously authorised uses in the EU, or that are based on obsolete Codex Maximum Residue Limits, or import tolerances that are not required any longer, EFSA proposed the lowering to the limit of quantification or to an alternative MRL. EFSA performed an indicative chronic and acute dietary risk assessment for the revised list of MRLs to allow risk managers to take the appropriate decisions.
Identifiants
pubmed: 37342544
doi: 10.2903/j.efsa.2023.8057
pii: EFS28057
pmc: PMC10277777
doi:
Types de publication
Journal Article
Langues
eng
Pagination
e08057Informations de copyright
© 2023 European Food Safety Authority. EFSA Journal published by Wiley‐VCH GmbH on behalf of European Food Safety Authority.
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