# The Medicines Act 1968 (Amendment) Regulations 1992, Regulation 3: Amendment of section 8 of the Act


(1) Section 8 of the Act(which contains provisions as to manufacture and wholesale dealing) shall be amended as follows.
(2) In subsection (3)(b) (under which a person who distributes certain medicinal products otherwise than by way of sale is required to have a wholesale dealer’s licence) for “or ready-made veterinary drug” there shall be substituted “, ready-made veterinary drug or industrially produced medicinal product other than a veterinary drug”.
(3) For subsection (4) (which applies definitions contained in section 7(7)) there shall be substituted—
“(4) Where the product which a person distributes is not a veterinary drug, subsection (3)(b) of this section shall not apply if the product is—
(a) whole human blood, human blood plasma or blood cells of human origin,
(b) a radiopharmaceutical in which the radionuclide is in the form of a sealed source, or
(c) a homoeopathic medicinal product.
(5) Where the product which a person distributes is a veterinary drug, subsection (3)(b) of this section shall not apply if the product is—
(a) a vaccine, toxin or serum,
(b) a product based on radioactive isotopes,
(c) a product specially prepared for administration by a veterinary surgeon or veterinary practitioner to a particular animal or herd which is under his care,
(d) a homoeopathic medicinal product, or
(e) an additive for animal feeding stuffs to which the provisions of Council Directive 70/524/EEC apply.
(6) In this section, “proprietary medicinal product”, “radiopharmaceutical” and “ready-made veterinary drug” have the same meanings as in section 7 of this Act.”.

---
Source: https://www.legislation.gov.uk/uksi/1992/604/regulation/3 (the official version)
Page: https://openlegislation.uk/medicines-act-1968-amendment-regulations-1992/regulation-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.