- Y Diweddaraf sydd Ar Gael (Diwygiedig)
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There are currently no known outstanding effects for the The Veterinary Medicines Regulations 2009 (revoked).
Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.
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
9.Incorporation of a veterinary medicinal product into feedingstuffs
10.Additional record keeping requirements relating to veterinary medicinal products
11.Labelling a premixture containing a veterinary medicinal product
12.Labelling of feedingstuffs containing a specified feed additive
13.Labelling of feedingstuffs containing a veterinary medicinal product
16.Supply of feedingstuffs containing a veterinary medicinal product
17.Prescriptions for feedingstuffs containing a veterinary medicinal product
24.Possession, placing on the market and use of feedingstuffs
27.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 an exceptional marketing authorisation (pharmaceutical)
13.Fees for an application for an exceptional marketing authorisation (immunological)
14.Fee for the conversion from an exceptional to a full marketing authorisation
15.Application for a marketing authorisation relating to a parallel import
16.Application for a variation obtained under a national procedure
17.Application for a variation to a marketing authorisation obtained through mutual recognition or decentralised procedures: fees until 1st January 2010
18.Application for a variation to a marketing authorisation obtained through mutual recognition or decentralised procedures: fees from 1st January 2010
19.Application for an extension to a marketing authorisation
20.Decentralised application for an extension where the United Kingdom is the reference member State
21.Provision of information relating to the recognition of a United Kingdom marketing authorisation
22.Application for the renewal of a national marketing authorisation
23.Application for the renewal of a marketing authorisation obtained through mutual recognition or the decentralised procedure
29.Application for a variation of a manufacturing authorisation
30.Application for an authorisation to manufacture an autogenous vaccine or a product for administration under the cascade
33.Inspection of a site where immunological veterinary medicinal products are manufactured
34.Inspection of a site where sterile veterinary medicinal products are manufactured
35.Inspection of a site where no immunological or sterile veterinary medicinal products are manufactured
36.Inspection of a site where veterinary medicinal products are assembled
38.Animal blood bank or equine stem cell centre authorisations
48.Importation of a veterinary medicinal product for treatment under the cascade
49.Importation of a veterinary medicinal product for administration under the Animals (Scientific Procedures) Act 1986
54.Appeals to the Veterinary Products Committee: marketing authorisations and animal test certificates
57.Appeal to the Veterinary Products Committee: active substance under Schedule 6
59.Fees relating to a veterinary surgeon’s practice premises
60.Refund of fees relating to the Veterinary Products Committee or appointed persons
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