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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2017/239    
Date of approval 03/03/2017 Expiration of approval 03/03/2027
RMS IE

Risk Assessment EFSA
Category FU Review Report   Approval 2016
  List of studies 2016
Remarks Admissible application according to Article 9 of Regulation (EC) No 1107/2009. Date of admissibility: 16/01/2014
Authorisation at national level
Authorised in In progress for
BE, IE, UK AT, CZ, ES, HU, IT, SI
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Oxathiapiprolin
    MRLs Annex II
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.14 Reg. (EU) 2017/239  
ARfD Not applicable Reg. (EU) 2017/239  
AOEL 0.04 Reg. (EU) 2017/239  
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