{
  "url": "https://openlegislation.uk/medicines-homoeopathic-medicinal-products-for-human-use-regulations-1994/regulation-7",
  "json_url": "https://openlegislation.uk/medicines-homoeopathic-medicinal-products-for-human-use-regulations-1994/regulation-7.json",
  "legislation": "uksi/1994/105",
  "legislation_title": "The Medicines (Homoeopathic Medicinal Products for Human Use) Regulations 1994",
  "legislation_url": "https://openlegislation.uk/medicines-homoeopathic-medicinal-products-for-human-use-regulations-1994",
  "path": "regulation/7",
  "kind": "regulation",
  "number": "7",
  "heading": "Requirements in respect of controls",
  "text": "The holder of a certificate of registration shall be responsible for furnishing to the licensing authority, on request, details of controls carried out on the finished product and, where applicable, on the ingredients of that product and of the controls carried out at an intermediate stage of the manufacturing process, in each case in accordance with the methods notified to the licensing authority at the time the certificate was applied for.",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [
    {
      "type": "rev",
      "affecting": "uksi/2005/2753",
      "affecting_title": "Medicines (Homoeopathic Medicinal Products for Human Use) Amendment Regulations 2005"
    }
  ],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/uksi/1994/105/regulation/7",
    "retrieved_at": "2026-10-29T13:42:46.380953+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."
}