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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
ES, FR, IT, PT NL
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