{
  "abstract": "In the United Kingdom (UK), the Medicines and Healthcare products Regulatory Agency (MHRA) 1 serves as the principal medicines regulatory authority, operating under the Human Medicines Regulations 2012.2 Its key role is to ensure that medicines are effective, safe and manufactured to consistently high standards.",
  "authors": [
    {
      "affiliations": [
        "House of Lords, London, London, UK"
      ],
      "name": "Ruslan Zinchenko"
    },
    {
      "affiliations": [
        "Institute of Pharmaceutical Science, King’s College London, London, UK"
      ],
      "name": "David Taylor"
    },
    {
      "affiliations": [
        "House of Lords, London, London, UK"
      ],
      "name": "Sheila Hollins"
    }
  ],
  "title": "Drug licensing in veterinary euthanasia and assisted suicide in humans: a regulatory double standard",
  "uid": "dd6b69b2-5aee-5fa2-a092-ac49b9d2b637"
}
