{
  "url": "https://openlegislation.uk/human-medicines-amendment-eu-exit-regulations-2021",
  "json_url": "https://openlegislation.uk/human-medicines-amendment-eu-exit-regulations-2021.json",
  "id": "uksi/2021/834",
  "title": "The Human Medicines (Amendment) (EU Exit) Regulations 2021",
  "short_title": "Human Medicines 2021",
  "long_title": "These Regulations amend the Human Medicines Regulations 2012 (“the HMRs”), which govern the arrangements throughout the United Kingdom for the manufacture, importation and marketing of medicinal products for human use. Regulation 3 of the HMRs contains exemptions from the manufacturing and product licensing requirements of the HMRs that relate to the manufacture or assembly of medicines by doctors, dentists, nurses and midwives at the final stage of the medicines supply chain – and related to those exemptions, there are provisions of regulation 3 that deal with the packaging, labelling and leafleting requirements for the products covered by those exemptions.",
  "citation": "S.I. 2021/834",
  "type": "uksi",
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      "heading": "Amendment of regulation 3 of the Human Medicines Regulations 2012",
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      "heading": "Amendment of the Human Medicines (Amendment etc.) (EU Exit) Regulations 2020",
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      "id": "ukpga/2018/16",
      "title": "European Union (Withdrawal) Act 2018",
      "url": "https://openlegislation.uk/european-union-withdrawal-act-2018",
      "provisions": [
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    "retrieved_at": "2026-10-28T22:10:56.102848+00:00"
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  "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."
}