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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2016/1425 ,
Reg. (EU) 540/2011
   
Date of approval 15/09/2016 Expiration of approval 15/09/2026
RMS BE

Risk Assessment EFSA
Category FU Review Report   Approval 2016
  List of studies relied upon
Remarks Admissible application according to Article 9 of Regulation (EC) No 1107/2009. Date of admissibility: 03/04/2013
Authorisation at national level
Authorised in In progress for
AT, CZ, EL, ES, HU, IT, SI
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Isofetamid
    MRLs Annex II
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.02 Reg. (EU) 2016/1425  
ARfD 1 Reg. (EU) 2016/1425  
AOEL 0.05 Reg. (EU) 2016/1425  
Other
 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level