94/505/EC: Commission Decision of 18 July 1994 amending the Decision of 18 December 1992 concerning the placing on the market of a GMO containing product, the vaccine Nobi-Porvac Aujeszky live (gI,tk), pursuant to Article 13 of Council Directive 90/220/EEC

• CELEX: Directive 90/220/EEC
• Articles: 2

Article 1

A favourable decision is hereby taken, according to which, the product Nobi-Porvac Aujeszky live, containing a genetically modified pseudorabies virus (strain Begonia) (gI , tk ) in a preparation with Diluvac Forte, modified by Vemie Veterinaer Chemie GmbH (Ref. C/D/92/I-1) and for which consent has been given by a Commission Decision of 18 December 1992 for the placing on the market as a live vaccine for Aujeszky disease to be administered by intra-muscular application only, shall now also be given consent for intra-dermal application as well.

Article 2

This Decision is addressed to the Member States.

Done at Brussels, 18 July 1994.

For the Commission

Yannis PALEOKRASSAS

Member of the Commission

(1) C (92) 3215 final.