The purpose of this Delegated Regulation is to supplement Regulation (EU) 2019/4 (Medicated Feed Regulation) by establishing, as regards the 24 antimicrobial active substances, specific maximum levels of cross-contamination for these substances in non-target feed and methods of analysis for these antimicrobial active substances in feed.
The maximum levels of cross-contamination are based on scientific risk assessments carried out by the European Food Safety Authority. The European Union Reference Laboratory for feed additives recommended methods of analysis for the above-mentioned 24 antimicrobial active substances in feed.
A cross-contamination level in non-target feed of 1% of the active substance in the medicated feed is proposed, based on experiences gained and representing a good balance between:
- the control of antimicrobial resistance and the levels causing effects on growth promotion or increased yield, based on the scientific opinions of the Authority;
- feasibility for the feed industry;
- enforceability by competent authorities.
Stricter limits are needed e.g. after the production of medicated feed for fish and to avoid residues in certain food. Furthermore, limits should apply in non-target feed in case of flushing with feed materials after production of medicated feed.
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