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 proficiency 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.
We have introduced glucocorticoids as new veterinary medicine residues in 2017.
Veterinary medicines are used across a range of livestock all around the world. Therefore the substantial impact reach which can be achieved through large scale poor farming practices requires effective testing processes from which to mitigate any risks to the consumer.
Fapas quality control materials are useful to ensure ongoing assessment of your testing ability. This can ensure your testing measures are maintained between proficiency testing activities, and in turn any improvements can be actioned accordingly to safeguard the testing ability of your laboratories and staff. This can be through both instrumentation calibration and staff training activities.
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