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

• CELEX: Implementing Regulation (EU) No 19/2014
• Articles: 3

Article 1

The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.

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 .

Schedules & Appendices

ANNEX

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.