{
  "url": "https://openlegislation.uk/eu-regulation-2019-6/article-89",
  "json_url": "https://openlegislation.uk/eu-regulation-2019-6/article-89.json",
  "legislation": "eur/2019/6",
  "legislation_title": "Regulation (EU) 2019/6 of the European Parliament and of the Council of 11 December 2018 on veterinary medicinal products and repealing Directive 2001/82/EC (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2019-6",
  "path": "article/89",
  "kind": "article",
  "number": "89",
  "heading": "Application for manufacturing authorisation",
  "text": "1. An application for a manufacturing authorisation shall be submitted to a competent authority in the Member State in which the manufacturing site is located.\n2. An application for a manufacturing authorisation shall contain at least the following information:\n(a) veterinary medicinal products which are to be manufactured or imported;\n(b) name or company name and permanent address or registered place of business of the applicant;\n(c) pharmaceutical forms which are to be manufactured or imported;\n(d) details about the manufacturing site where the veterinary medicinal products are to be manufactured or imported;\n(e) a statement to the effect that the applicant fulfils the requirements laid down in Articles 93 and 97.",
  "extent": "E+W+S+N.I.",
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eur/2019/6/article/89",
    "retrieved_at": "2026-11-01T14:43:40.425754+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."
}