Commission Implementing Regulation (EU) No 497/2012
of 7 June 2012
amending Regulation (EU) No 206/2010 as regards the requirements for imports of animals susceptible to bluetongue
(Text with EEA relevance)
THE EUROPEAN COMMISSION,
Having regard to the Treaty on the Functioning of the European Union,
Whereas:
In particular, with regard to animals susceptible to bluetongue, certificates BOV-X, BOV-Y, OVI-X, OVI-Y and RUM set out in Part 2 of Annex I to Regulation (EU) No 206/2010 include inter alia the requirement that the animals come from a territory which, at the date of issue of the certificate accompanying them had been free from bluetongue for a period of twelve months.
As a result of new technical developments, "inactivated vaccines" against bluetongue have become available which do not pose the risk of undesired local circulation of the vaccine virus to unvaccinated cattle, sheep and goats. It is now widely accepted that vaccination with inactivated vaccines is the preferred tool for the control of bluetongue and for the prevention of clinical disease in such animals in the Union.
Accordingly, Directive 2000/75/EC now provides for the use of inactivated vaccines in all parts of the EU.
Directive 2000/75/EC and Regulation (EC) No 1266/2007 apply to intra-Union movements of live ungulates of species susceptible to bluetongue. It is appropriate that the models of veterinary certificates BOV-X, BOV-Y, OVI-X, OVI-Y and RUM set out in Part 2 of Annex I to Regulation (EU) No 206/2010 be amended to align the animal health requirements for imports into the Union, as regards bluetongue, to the requirements for intra-Union movement in animals susceptible to that disease.
Regulation (EU) No 206/2010 should therefore be amended accordingly.
The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS REGULATION: