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
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
Directive 90/220/EEC Β· Decision Β· 2 articles
Data as of 2026-07-04 Β· Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. Β· Read the official text β
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.
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.
