The Veterinary Medicines (Amendment) Regulations 2014

• Citation: S.I. 2014/599
• Sections: 4

Section 1 Title and commencement

These Regulations may be cited as the Veterinary Medicines (Amendment) Regulations 2014 and come into force on 14th April 2014.

Section 2 Amendments of the Veterinary Medicines Regulations 2013

The Veterinary Medicines Regulations 2013 are amended in accordance with Regulations 3 to 6.

Section 3 Amendment of Schedule 5

(1) Schedule 5 (medicated feedingstuffs and specified feed additives) is amended as follows.

(2) In paragraph 20 (writing the prescription) for sub-paragraph (3) substitute—

(3) The person must prescribe a veterinary medicinal product authorised for incorporation in feedingstuffs but may, if there is no veterinary medicinal product authorised for a condition in a particular species—

(a) prescribe a veterinary medicinal product authorised for another species or for another condition in the same species, and

(b) prescribe more than one veterinary medicinal product,

provided all veterinary medicinal products prescribed are authorised for incorporation in feedingstuffs.

(3) In paragraph 29 (import for incorporation into premixture or feedingstuffs for export) for sub-paragraph (1) substitute—

(1) A manufacturer of premixture or feedingstuffs who imports a veterinary medicinal product authorised in another Member State or third country for the purposes of incorporating it into premixture or feedingstuffs for export does not commit an offence under regulation 43(q) (importation of an unauthorised veterinary medicinal product) or regulation 43(r) (possession of an unauthorised veterinary medicinal product)

(4) In paragraph 31(q) (prescription writing offences) for the words “20(1) or (2)” substitute “20”.

Section 4 Amendment of Schedule 7

(1) Schedule 7 is amended as follows—

(2) In Part 2 (fees relating to marketing authorisations) in paragraph 17 (application for a variation to a marketing authorisation dealt with under national or mutual recognition variation procedures) in paragraph (i) of the entry in the table relating to the change of route of administration or the addition of a new one, for the word “food-producing” substitute “non-food-producing”.

(3) In Part 6 (general) in paragraph 50 (wholesale dealer’s import certificate) for “£1,320” substitute “£760”.

(4) In Part 6 (general) for paragraph 51 (specific batch control) substitute—

(51) The fee for an authorisation to release a veterinary medicinal product under specific batch control is—

(a) £560; and

(b) £100 for each additional batch affected by the same issue where the specific batch control application is made at the same time.