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| Product Code | Material | Matrix | Approx. Size |
|---|---|---|---|
|
FCVD24-MRP6QC
|
T02489QC |
Bovine Kidney |
25 g |
Diclofenac, Tolfenamic Acid
10/07/2025
This quality control material evaluates veterinary drugs, specifically NSAIDs in Bovine Kidney.
Veterinary medicines used in animals have a wide range of effects in humans. Hence, many veterinary medicines have extremely low maximum residue limits (MRLs) or even no limit, where any detection is classed as non-compliant. The Fapas quality control materials are produced in keeping with EU MRLs or minimum required performance limit (MRPL) where MRLs are not set.
The result reporting requirements are also in keeping with quality control guidelines laid out in EC/657/2002.
Animal products for human consumption are tightly legislated and closely monitored for compliance. Veterinary medicines used in animals are likely to have a pharmacological effect in humans. Hence, for many veterinary medicines, there are extremely low maximum residue limits or even no MRL (i.e. any detection is non-compliant). The Fapas test materials are produced in keeping with EU MRLs or minimum required performance limit (MRPL) where MRLs are not set. The result reporting requirements are also in keeping with quality control guidelines laid out in EC/657/2002. Fapas veterinary medicine test materials include incurred residues, as well as fortified animal products, and are suitable for all methods, including screening methods (for the detection of the total amount of that chemical class).
Quality control materials from Fapas make use of real food matrices, from which to ensure direct comparisons can be made with your current routine analysis activities. This can ensure any areas of improvement are relevant and concise to action in an efficient way, to pass directly to your customers and regulators alike. These are invaluable to ensure your testing ability is competitive within a saturated business environment.
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