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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/66 ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2009 Expiration of approval 31/12/2018
RMS

Co-RMS
SE

DE
Risk Assessment EFSA
Category AL, HB Review Report
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, DK, FR, HU, IE, LU, NL, PL, SK, UK SE
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Quinoclamine
    MRLs Annex V
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.002 Dir 08/66  
ARfD 0.05 Dir 08/66  
AOEL 0.03 Dir 08/66  
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