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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 02/48/EC ,
Reg. (EU) 2016/147 ,
Reg. (EU) No 540/2011
Old Legislation 2010/77/EU ,
Reg. (EU) 2015/1885
Date of approval 01/04/2016 Expiration of approval 31/03/2031
RMS

Co-RMS
IE

IT
Risk Assessment EFSA
Category FU Review Report   Confirmatory data 2018
  List of studies (Revised) 2017
  Renewal 2016
  Inclusion 2002
Authorisation at national level
Authorised in In progress for
AT, BG, CY, CZ, DE, EL, ES, FR, HR, HU, IT, MT, PT, RO, SI, SK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Iprovalicarb
    MRLs Annex II
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.015 Reg. (EU) 2016/147  
ARfD Not applicable Reg. (EU) 2016/147  
AOEL 0.015 Reg. (EU) 2016/147  
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