Article 1
The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
Commission Implementing Regulation (EU) 2026/1806 of 24 July 2026 amending Regulation (EU) No 37/2010 as regards the classification of the substance recombinant equine chorionic gonadotropin with respect to its maximum residue limit in foodstuffs of animal origin
Commission Implementing Regulation (EU) 2026/1806 of 24 July 2026 amending Regulation (EU) No 37/2010 as regards the classification of the substance recombinant equine chorionic gonadotropin with respect to its maximum residue limit in foodstuffs of animal origin
Data as of 2026-08-20 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗
Article 2
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union .
Supplementary provisions
ANNEXSupplementary provisions
ANNEX In Table 1 of the Annex to Regulation (EU) No 37/2010, the following entry is inserted in alphabetical order: Pharmaco-logically active substance Marker residue Animal species MRL Target Tissues Other provisions (according to Article 14(7) of Regulation (EC) No 470/2009) Therapeutic classification ‘Recombinant equine chorionic gonadotropin (reCG, recombinant analogues of pregnant mare serum gonadotrophin) – chemical-unlike biological substance NOT APPLICABLE All food-producing species No MRL required NOT APPLICABLE NO ENTRY NO ENTRY’
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