Core Competencies

  • Human Food Safety drug development programs for veterinary drugs
  • Technical and regulatory support to establish Maximum Residue Levels (USFDA tolerances; MRLs, Codex, EMA, Canada)
  • In vitro and in vivo drug metabolism
  • Analytical method development and validation for bioanalytical methods and tissue residues.
    • GLP validation of Animal Health Drug Residue Methods
    • AOAC published tissue residue methods
    • Bioanalytical validation support for regulated industry (cannabis control methods)
  • Drug residue analysis, pharmacokinetics and tissue residue decline.
  • Special expertise in methodology for bovine somatotropin (bST) methods in plasma and milk.
  • Regulatory support of safety standards, providing a technical interface between drug company, producers and regulatory agencies.
  • Cross-functional scientific leadership in Knowledge Management / Communities of Practice in order to encourage collaboration and career development.