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) No 19/2014 of 10 January 2014 amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance chloroform Text with EEA relevance
Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗
The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union .
ANNEX The Annex to Regulation (EU) No 37/2010 is amended as follows: (1) in Table 1 the substance chloroform is inserted as follows: Pharmacologically active Substance Marker residue Animal Species MRL Target Tissues Other Provisions ( according to Article 14(7) of Regulation (EC) No 470/2009 ) Therapeutic Classification ‘Chloroform NOT APPLICABLE All mammalian food producing species No MRL required NOT APPLICABLE Only to be used as an excipient in vaccines and only at concentrations not exceeding 1 % w/v and total doses not exceeding 20 mg per animal. NO ENTRY’ (2) in Table 2 the substance chloroform is deleted.
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