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Commission Regulation (EC) No 1234/2008 ANNEX V

Commission Regulation (EC) No 1234/2008 ANNEX V

ANNEX VSupplementary provisions

ANNEX V PART 1 Variations concerning a change to or addition of therapeutic indications. PART 2 1.   Variations concerning a change to or addition of a non-food producing target species. 2.   Variations concerning the replacement or addition of a serotype, strain, antigen or combination of serotypes, strains or antigens for a veterinary vaccine against avian influenza, foot-and-mouth disease or bluetongue. 3.   Variations concerning the replacement of a strain for a veterinary vaccine against equine influenza.

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Other provisions in Commission Regulation (EC) No 1234/2008

Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗ · Data as of 2026-07-04

CitationANNEX V of Commission Regulation (EC) No 1234/2008 (LawPlayer, data as of 2026-07-04)

© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.

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