Regulation 130 Amendment to paragraph 7

In paragraph 7 (approval of manufacturers and distributors of feedingstuffs containing veterinary medicinal products)—

(a)

in sub-paragraph (2)—

(i)

for “veterinary medicinal product”, in each place it occurs, substitute “medicinal premix”;

(ii)

for “a premixture” substitute “an intermediate feedingstuff”;

(iii)

for “premixtures” substitute “intermediate feedingstuffs”;

(iv)

for “approved” substitute “authorised”;

(b)

in sub-paragraph (3)—

(i)

for “approval”, in both places it occurs, substitute “authorisation”;

(ii)

for “establishments” substitute “premises”;

(c)

in sub-paragraph (4) for “approved” substitute “authorised”;

(d)

for sub-paragraph (5) substitute—

“(5)

A manufacturer must ensure that, so far as is reasonably practical the medicinal premix is evenly incorporated and homogeneously dispersed throughout the feedingstuffs, taking into account the specific properties of the medicinal premix and the mixing technology employed.”;

(e)

in sub-paragraph (6) for “veterinary medicinal product” substitute “medicinal premix”;

(f)

in sub-paragraph (7) for “approval” substitute “authorisation”;

(g)

in the heading—

(i)

for “Approval” substitute “Authorisation”;

(ii)

for “veterinary medicinal products” substitute “medicinal premixes”.