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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2017/157 ,
Reg. (EU) No 540/2011
Old Legislation 01/21/EC ,
2010/77/EU ,
Reg. (EU) 2015/1885 ,
Reg. (EU) 2016/549
Date of approval 01/04/2017 Expiration of approval 31/03/2032
RMS

Co-RMS
ES

NL
Risk Assessment EFSA
Category FU Review Report   Review Report 2016
  List of studies relied upon (AIR 2)
  Inclusion 2001
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, DE, EL, ES, FR, HR, HU, IE, IT, LU, PT, RO, SI, UK SK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Thiabendazole (R)
    MRLs Annex II
Classification Reg. 1272/2008
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.10 Reg. (EU) 2017/157  
ARfD 0.10 Reg. (EU) 2017/157  
AOEL 0.07 Reg. (EU) 2017/157  
Other
ADI 0,1 ARfD 0.3 (women of child-bearing age) JMPR 2006 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level