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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 03/84/EC ,
Reg. (EU) 2016/950 ,
Reg. (EU) 2017/1455 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012
   
RMS

Co-RMS
CZ

RO
Risk Assessment Commission
Category FU Review Report   Renewal Report 2017
  Inclusion 2003
Remarks Non-approval: Reg. (EU) 2017/1455

The original RMS was Ireland.
Authorisation at national level
Authorised in In progress for
BE, BG, CZ, EE, EL, FI, FR, IE, PL, PT, SE, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Picoxystrobin (F)
    MRLs Annex II
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.043 03/84/EC  
ARfD Not applicable 03/84/EC  
AOEL 0.043 03/84/EC  
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