Part I INTERPRETATION

In this Schedule—

• “application for a type A marketing authorisation” means an application for a marketing authorisation to which regulation 5(a) of the 1994 Regulations applies and “type A marketing authorisation” shall be construed accordingly;

• “application for a type B marketing authorisation” means an application for a marketing authorisation to which regulation 5(b) of the 1994 Regulations applies and “type B marketing authorisation” shall be construed accordingly;

• “Article 15.2 marketing authorisation” means a marketing authorisation of the type specified in Article 15.2 of Directive 81/851/EEC;

• “category I application” means an application for assistance in connection with a mutual recognition application other than a category II or III application;

• “category II application” means an application, other than a category III application, for assistance in connection with a mutual recognition application relating to a marketing authorisation granted in respect of a Veterinary Medicinal Product only intended for administration to animals whose flesh or products are not intended for human consumption;

• “category III application” means an application for assistance in connection with a mutual recognition application relating to a marketing authorisation granted in respect of an immunological Veterinary Medicinal Product;

• “food-producing animals” means animals whose flesh or products are intended for human consumption;

• “type I variation—Administrative” means a variation of the type listed in paragraphs 2 and 3 of Annex I to Regulation (EC) No. 541/95^f1;

• “type I variation—Scientific” means a variation of the type listed in paragraphs 1 and 4 to 33 of Annex 1 to Regulation (EC) No. 51/95; and

• “type II variation” means a variation of the type referred to in Article 3.1(b) of Regulation (EC) No. 541/95.