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Ordinance Amending The Ordinance On Veterinary Use, Dispensing And Prescribing Of Medicines For Animals

Original Language Title: Bekendtgørelse om ændring af bekendtgørelse om dyrlægers anvendelse, udlevering og ordinering af lægemidler til dyr

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Publication of the amendment of the notice of the use, extradition and prescribing of medicinal products for animals

(Identification of animals of the lifting of the horse as well as administrative lettings for the industry)

§ 1

Notice no. 482 of 29. May 2007 on the use, extradition and prescribing of medicinal products to animals as amended by the notice of publication No 2 ; 1286 of 15. In December 2008, the following changes are made :

1. I § 2, nr. 4, ' animal of the equidae ' is replaced by : ' Animals of the herder (hereafter referred to as horses) `.

2. Section 3, paragraph 3. 11, ITREAS :

" Stop. 11. The microchip means a transponder, as defined in Article 2 (1). 2, lira b) in Commission Regulation (EC) No 504/2008 of 6. June 2008 on the implementation of Council Directive 90 /426/EEC and 90 /427/EEC in respect of methods for the equidae of equidae. `

3. Section 26 (1). ONE, TWO. pkt., ITREAS :

' The test samples shall be taken by a veterinarian, one of the quality of the Danish Queses or the Animal owner himself. ' ;

4. I the title of Chapter 10 ; the ' equidae ` shall be replaced by ' horses `.

5. I § 30, the ' equidae ` shall be replaced by ' horses `.

6. I Section 31 (1). 1, the ' equidae ` shall be replaced by ' horses `.

7. Section 31 (1). 2, ITREAS :

" Stop. 2. The veterinarian shall be treated for the treatment of horses in accordance with paragraph 1. 1, within the context of the treatment mark the horse with microchip (transponder). The implant is implanted at the centre of the neck in the middle of the neck between the neck and the mane in the transition between muscle and spasm, cf. Article 11 (1). TWO, ONE. section of Commission Regulation (EC) No 504/2008 of 6. June of the implementation of Council Directive 90 /426/EEC and 90 /427/EEC in the case of methods for the identification of equidae. The transponder must be put on the left side of the horse's neck. "

8. Section 31 (1). 4, ITREAS :

" Stop. 4. In the context of the treatment, the veterinary certification and the animal owner, with his signature, confirm that the treatment excludes the horse from the use for human consumption. "

9. Section 31 (1). 5 and 6, deleted.

10. I § 31 the following paragraphs are added :

" Stop. 5. If the horse has a passport, the veterinarian in relation to the treatment must complete the passage of the passage, cf. Article 20 of the paragraph in paragraph 1. 2 mentioned Regulation.

Paragraph 6. If the horse does not have a passport, the veterinarian must, in the context of the treatment, complete the form ' Declaration on the exclusion of human consumption from which it is to be requested from, and the veterinarian in a solid condition is returned to the Danish Agricultural Advisory Committee, the Rural Centre ; Horses, at the same time at the request of the owner to issue a passport to the horse, cf. Article 5 of the paragraph in paragraph 1. 2 mentioned Regulation. The veterinarian must return the declaration no later than two days after the treatment. `

11. Section 31 (1). 7, ITREAS :

" Stop. 7. Horses before the entry into force of this notice have been excluded from human consumption shall continue to be accompanied by a 'Veterinary and Owning Animal Family Animal Health certificate treated with medicinal products excluding the animal from human consumption' until such time as there is issued a passport for the horse in accordance with the provisions referred to in paragraph 1. This Regulation shall show the exclusion of the horse from which the horse is excluded from human consumption. In the process of re-examination, as described in paragraph 1, The horse shall, on the occasion of the owner, be provided with a passport in accordance with the provisions laid down in paragraph 1. The Regulation shall be referred to.

§ 2

The announcement shall enter into force on 1. January, 2010.

The FDA, the 15th. December 2009Jan Mousing / Kirsten Sejlstrup