Note: Fees (prices) on this site are in GBP and do not include carriage / handling fees and VAT. Customers outside the UK may also incur local charges, including (but not limited to) import duties, local taxes and customs clearance fees, which may add significant cost to your order. Prices here are for the PT round or QC / Reference Material only and the total price payable may be higher.
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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 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. Fapas veterinary medicine quality control 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).
The ability to achieve large amounts of high-quality livestock to satisfy global demand is important to ensure large financial rewards are safeguarded for producers. This can lead to poor farming practices being utilised to ensure financial rewards are met, which can increase the risk of high levels of veterinary medicine residues being passed on to the end consumer, which can prove harmful to health in some instances.
Fapas quality control materials make use of real food matrices from which to ensure direct comparisons can be made between your routine analysis and quality control results. From these insights your testing abilities can be safeguarded across the year to ensure the accuracy of your results is maintained through staff training activities and instrumentation calibration activities.
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