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162. In paragraph 1 (interpretation)—
(a)the existing text is renumbered as sub-paragraph (1);
(b)in sub-paragraph (1), in the definition of “pharmaceutical product”, at the end insert “or a biological veterinary medicinal product that is not immunological”;
(c)after that sub-paragraph insert—
“(2) For the purposes of this Schedule “manufacturing authorisation” means the following activities—
(a)manufacture or import of an authorised veterinary medicinal product;
(b)manufacture of a product to which paragraph 2 of Schedule 6 relates;
(c)manufacture of a product for administration under the cascade;
(d)manufacture of—
(i)an autogenous vaccine;
(ii)a stem cell product; or
(iii)a blood product for administration to non-food animals.”.
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