{
  "url": "https://openlegislation.uk/medicines-veterinary-medicinal-products-applications-for-product-licences-regulations-1993/regulation-3",
  "json_url": "https://openlegislation.uk/medicines-veterinary-medicinal-products-applications-for-product-licences-regulations-1993/regulation-3.json",
  "legislation": "uksi/1993/2398",
  "legislation_title": "The Medicines (Veterinary Medicinal Products) (Applications for Product Licences) Regulations 1993",
  "legislation_url": "https://openlegislation.uk/medicines-veterinary-medicinal-products-applications-for-product-licences-regulations-1993",
  "path": "regulation/3",
  "kind": "regulation",
  "number": "3",
  "heading": "Form and manner of application",
  "text": "(1) Every application shall be made in writing in the English language and shall be signed by the applicant.\n(2) The applicant shall supply to the licensing authority four copies of each application, and shall supply a further twenty-two copies if the licensing authority so directs.\n(3) Where the application, or any part thereof, has been translated from another language, the applicant shall supply to the licensing authority one copy of such application or part, as the case may be, in the original language if the licensing authority so directs.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/uksi/1993/2398/regulation/3",
    "retrieved_at": "2026-10-29T13:50:12.688736+00:00"
  },
  "licence": "Open Government Licence v3.0",
  "licence_url": "https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/",
  "attribution": "Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives."
}