OpenLegislation

Division 9 F1

United Kingdom

Original text. Later amendments are not shown.

The environmental risk assessment connected with the release of veterinary medicinal products containing or consisting of Genetically Modified Organisms (GMOs) within the meaning of Article 2 of Directive 2001/18/EC of the European Parliament and of the Council f1 shall be provided in the dossier. The information shall be presented in accordance with the provisions of Directive 2001/18/EC and Regulation (EC) No 726/2004 of the European Parliament and of the Council f2 , taking into account guidance documents published by the Commission.

Annotations

Textual amendments

F1

Substituted by Commission Directive 2009/9/EC of 10 February 2009 amending Directive 2001/82/EC of the European Parliament and of the Council on the Community code relating to medicinal products for veterinary use (Text with EEA relevance).

Footnotes

f1

OJ L 106, 17.4.2001, p. 1 .

f2

OJ L 136, 30.4.2004, p. 1 .