Regulation on Residue Tolerances for Veterinary Medicinal Products
PROPOSAL FOR A COUNCIL REGULATION(EEC)LAYING DOWN A COMMUNITY PROCEDURE FOR THE ESTABLISHMENT OF TOLERANCES FOR RESIDUES OF VETERINARY MEDICINAL PRODUCTS
- Stage
- No longer in force
- Procedure
- Regulation · Consultation procedure
- Last activity
- 1 Jan 1992
Summary
GeneratedCouncil Regulation (EEC) No 2377/90 sets EU maximum residue limits for pharmacologically active substances in food of animal origin, sorting substances into Annexes I–IV. It entered into force on 1 January 1992; from 1 January 1997, administering substances not listed in Annexes I, II or III to food-producing animals was prohibited. It binds member states and marketing authorization holders.
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Sources: EP Legislative Observatory · EU Law Tracker · EUR-Lex. Record as of 27 Oct 2026. Something wrong on this page? Report an error.
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