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3.—(1) Section 8 of the Act (manufacture and wholesale dealing) shall be amended in accordance with this regulation.
(2) For subsection (3) (wholesale dealer's licence) there shall be substituted the following subsections—
“(3)
(a)sell, or offer for sale, any medicinal product by way of wholesale dealing, or
(b)distribute, otherwise than by way of sale, any proprietary medicinal product which has been imported, but was not consigned from a member State,
except in accordance with a licence granted for the purposes of this subsection (in this Act referred to as a “wholesale dealer's licence”).
(4) In this section—
(a)“proprietary medicinal product” means
(b)for the purposes of paragraph (a) “medicinal product”
(i)vaccines, toxins or serums,
(ii)medicinal products based on human blood or blood constituents or radioactive isotopes,
(iii)homoeopathic medicinal products, or
(iv)veterinary drugs.”.
(3) This regulation shall come into force on 1st September 1977.
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