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Residues consumer risk

Residue data are required as part of regulatory submissions for approval/renewal of active substances as well as for the authorization of biocides and phytopharmaceutical products in the EU.

Our residues experts provide a full range of support services for:

  • Dossier preparation – assessing the risk to humans through food following acute or chronic exposure, according to the European requirements and based on the existing guidance documents (from ECHA and EMA for biocides)
  • Scientific waivers/justification
  • Ad-hoc technical documents for specific requirements
  • MRL/Import Tolerance Applications
  • Non-EU MRLs/JMPR Periodic Reviews and Codex MRL (CXL) Setting
  • Study set-up and monitoring of GLP studies