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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2015/1106 ,
Reg. (EU) No 1037/2012
Old Legislation Dossier complete 2010/132/EU
Date of approval 01/04/2013 Expiration of approval 31/03/2023
    Risk Assessment EFSA
Category FU Review Report
Remarks Timelines for submission of confirmatory information amended. Proposal voted at PAFF in June 2015.

The original RMS was UK.

The RMS is Norway
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, CY, CZ, DE, EL, HR, HU, IE, IT, LU, NL, PL, RO, SI, SK, UK BG, ES, SE
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Isopyrazam
    MRLs Annex IIIA
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.03 EFSA 12  
ARfD 0.2 EFSA 12  
AOEL 0.05 EFSA 12  
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