{
  "url": "https://openlegislation.uk/marketing-authorisations-for-veterinary-medicinal-products-regulations-1994",
  "json_url": "https://openlegislation.uk/marketing-authorisations-for-veterinary-medicinal-products-regulations-1994.json",
  "id": "uksi/1994/3142",
  "title": "The Marketing Authorisations for Veterinary Medicinal Products Regulations 1994",
  "short_title": "Marketing Authorisations for Veterinary Medicinal Products 1994",
  "long_title": "These Regulations implement Council Directive 93/40/EEC, which is the latest in a series of amendments to Council Directive 81/851/EEC. They provide for veterinary medicinal products to be placed on the market subject to marketing authorisations rather than the previous system of product licences. These authorisations may be granted either by the Ministers or, in accordance with Council Regulation 2309/93/EEC, by the European Agency for the Evaluation of Medicinal Products (regulation 3).",
  "citation": "S.I. 1994/3142",
  "type": "uksi",
  "year": "1994",
  "number": "3142",
  "version": "current",
  "date": "1994-12-05",
  "revised": false,
  "valid_from": null,
  "extent": null,
  "unapplied_effects": 35,
  "provisions": [
    {
      "path": "introduction",
      "kind": "introduction",
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      "heading": "Introductory text",
      "url": "https://openlegislation.uk/marketing-authorisations-for-veterinary-medicinal-products-regulations-1994/introduction",
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      "heading": "Circumstances in which these Regulations do not apply",
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      "heading": "Placing veterinary medicinal products on the market",
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      "heading": "Form and manner of application",
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      "heading": "Grant of an authorisation",
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      "heading": "Duties on persons responsible for placing products on the market",
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      "heading": "Products manufactured outside the European Economic Area",
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      "path": "regulation/18",
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      "heading": "Application of the Medicines Act 1968, the Trade Descriptions Act 1968 and the Consumer Protection Act 1987 to marketing authorisations",
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      "heading": "Signature",
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      "heading": "REQUIREMENTS IN RESPECT OF PRODUCTS OTHER THAN IMMUNOLOGICAL PRODUCTS",
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