Reliable analysis of veterinary drug residues in animal-derived foodstuffs represents an important measure to ensure consumer protection. European Legislation addresses this issue, for instance by defining maximum residue level, specifying sampling and monitoring plans, and stipulating performance and validation criteria for analytical methods. Certified reference materials (CRMs) constitute an important tool for method validation and method performance verification. This article addresses the current status of legislation, describes characteristics of analytical methods in veterinary drug residue testing and then focuses on the challenges and considerations towards the development of new (certified) reference materials in this field
ZELENY Reinhard;
ULBERTH Franz;
EMONS Hendrik;
GOWIK Petra;
POLZER Joachim;
VAN GINKEL Leendert A.;
2006-10-06
ELSEVIER
JRC33436
https://publications.jrc.ec.europa.eu/repository/handle/JRC33436,
10.1016/j.trac.2006.04.011,
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