{
  "url": "https://openlegislation.uk/medicines-products-for-human-use-fees-regulations-2012/schedule-5",
  "json_url": "https://openlegislation.uk/medicines-products-for-human-use-fees-regulations-2012/schedule-5.json",
  "legislation": "nisr/2012/134",
  "legislation_title": "The Medicines (Products for Human Use) (Fees) Regulations 2012",
  "legislation_url": "https://openlegislation.uk/medicines-products-for-human-use-fees-regulations-2012",
  "path": "schedule/5",
  "kind": "schedule",
  "number": "5",
  "heading": "FEES FOR CERTIFICATES OF REGISTRATION",
  "text": "Column (1)\nColumn 2\nColumn 3\nType of application\nFees for applications in respect of products prepared from not more than 5 homoeopathic stocks\nFees for other applications\n1\nAn application in respect of a product which is both prepared solely from repeat stocks and is of a repeat formulation.\n£172\n£425\n2\nAn application in respect of a product which is either—\n£517\n£761\n(a)\nprepared solely from repeat stocks; or\n(b)\nis of a repeat formulation.\n3\nA mutual recognition procedure incoming application.\n£542\n£690\n4\nA mutual recognition outgoing application (regulatory assistance).\n£310\n£405\n5\nA decentralised procedure application where the UK is a concerned Member State.\n£465\n£608\n6\nA decentralised procedure application where the UK is the reference Member State.\n£930\n£1,217\n7\nAny other application.\n£854\n£1,118",
  "extent": null,
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/nisr/2012/134/schedule/5",
    "retrieved_at": "2026-10-29T01:16:38.443269+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."
}