17.Food-producing animals: proof of purchase of veterinary medicinal products
18.Food-producing animals: records of administration by a veterinary surgeon
19.Food-producing animals: records of acquisition and administration
22.Records by a holder of a wholesale dealer’s authorisation
23.Records of the receipt or supply of prescription products
24.Records of products administered to a food-producing animal under the cascade
The manufacture of veterinary medicinal products
Administration of a veterinary medicinal product outside the terms of a marketing authorisation
Medicated feedingstuffs and specified feed additives
6.Approval of manufacturers and distributors of feedingstuffs containing veterinary medicinal products
7.Incorporation of a veterinary medicinal product into a premixture
8.Incorporation of a veterinary medicinal product into feedingstuffs
9.Additional record keeping requirements relating to veterinary medicinal products
10.Labelling a premixture containing a veterinary medicinal product
11.Labelling of feedingstuffs containing a specified feed additive
12.Labelling of feedingstuffs containing a veterinary medicinal product
15.Supply of feedingstuffs containing a veterinary medicinal product
16.Prescriptions for feedingstuffs containing a veterinary medicinal product
23.Possession, placing on the market and use of feedingstuffs
26.Import for incorporation into premixture or feedingstuffs for export
8.Decentralised pharmaceutical application where the United Kingdom is the reference member State
9.Application for a marketing authorisation for an immunological product
10.Decentralised immunological application where the United Kingdom is the reference member State
11.Application for a marketing authorisation using identical data
12.Application for a provisional marketing authorisation (pharmaceutical)
13.Fees for an application for a provisional marketing authorisation (immunological)
14.Fee for the conversion from a provisional to a full marketing authorisation
15.Application for a marketing authorisation relating to a parallel import
17.Application for a variation to a marketing authorisation that has been issued in other member States
18.Application for an extension to a marketing authorisation
19.Decentralised application for an extension where the United Kingdom is the reference member State
20.Provision of information relating to the recognition of a United Kingdom marketing authorisation
21.Application for the renewal of a national marketing authorisation
22.Application for the renewal of a marketing authorisation granted in more than one member State
28.Application for a variation of a manufacturing authorisation
29.Application for an authorisation to manufacture an autogenous vaccine or a product for administration under the cascade
32.Inspection of a site where immunological veterinary medicinal products are manufactured
33.Inspection of a site where sterile veterinary medicinal products are manufactured
34.Inspection of a site where no immunological or sterile veterinary medicinal products are manufactured
35.Inspection of a site where veterinary medicinal products are assembled
37.Animal blood bank or equine stem cell centre authorisations
48.Treatment under the Animals (Scientific Procedures) Act 1986
53.Appeals to the Veterinary Products Committee: marketing authorisations and ATCs
56.Appeal to the Veterinary Products Committee: active substance under Schedule 6
58.Fee for the inspection of a veterinary surgeon’s practice premises
58A.Fee for the registration of veterinary practice premises
59.Refund of fees relating to the Veterinary Products Committee or appointed persons