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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 07/6/EC ,
Reg. (EU) 2015/1396 ,
Reg. (EU) No 2018/524 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) No 487/2014
Date of approval 01/02/2007 Expiration of approval 30/04/2019
RMS

Co-RMS
DE

DK
Risk Assessment Commission
Category BA, FU Review Report
Remarks Extention of approval (Reg (EU) 2018/524)
Conditions of approval amended.
Authorisation at national level
Authorised in In progress for
BE, CY, CZ, DE, DK, EE, EL, ES, FI, FR, IE, IT, LT, LU, LV, NL, PL, PT, SE, SI, SK, UK AT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Bacillus subtilis strain QST 713
    MRLs Annex IV
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI Not applicable 07/6/EC  
ARfD Not applicable 07/6/EC  
AOEL Not applicable 07/6/EC  
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