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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 17/2013 Old Legislation Dossier complete 08/565/EC
Date of approval 01/06/2013 Expiration of approval 31/05/2023
RMS

Co-RMS
IT

SK
Risk Assessment EFSA
Category FU Review Report
Remarks The original RMS was France.
Authorisation at national level
Authorised in In progress for
FR IT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Trichoderma atroviride strain I-1237
    MRLs Annex IV
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI Not applicable EFSA 12  
ARfD Not applicable EFSA 12  
AOEL Not applicable 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