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
PART 5 Miscellaneous provisions, enforcement and offences
PART 4 Variations of marketing authorisations on the application of the holder
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
PART 2 Fees relating to marketing authorisations
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
PART 3 Fees payable by manufacturers
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
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.Refund of fees relating to the Veterinary Products Committee or appointed persons