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Animal law, horse law and animal liability in Germany

Medicated feed in 2026: homogeneity and cross-contamination

The Commission’s March 2026 guidance makes production controls a practical priority for feed businesses.

Published 8 November 2026

What changed

On 19 March 2026 the European Commission published guidance on evaluating feed homogeneity and cross-contamination. It addresses how competent authorities assess the methods used by feed businesses. Guidance should be read alongside Regulation (EU) 2019/4 and the relevant binding measures, including Regulation (EU) 2024/1229.

What to check in the business

Map the production lines, substances and products concerned. Review sampling plans, carry-over testing, cleaning validation, batch-release responsibilities and the records supporting each decision. A technical method that works in one production setting may not be appropriate for another.

Contract and inspection implications

Contract manufacturers and brand owners should agree who provides test evidence, investigates deviations and makes recall decisions. If an authority challenges a result, preserve the sampling chain and analytical method as well as the final number. Our practical recommendation is to carry out the legal and technical review together.

When advice is useful

Seek a review before a new production arrangement, following a material test failure or when an inspection questions existing controls. The response should distinguish an evidential disagreement from a product-safety concern requiring immediate action.

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Medicated feed in 2026: homogeneity and cross-contamination

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