{
  "url": "https://openlegislation.uk/eu-regulation-2019-6/article-96",
  "json_url": "https://openlegislation.uk/eu-regulation-2019-6/article-96.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/96",
  "kind": "article",
  "number": "96",
  "heading": "Record keeping",
  "text": "1. The holder of a manufacturing authorisation shall record the following information in respect of all veterinary medicinal products that it supplies:\n(a) date of the transaction;\n(b) name of the veterinary medicinal product, and marketing authorisation number if applicable, as well as pharmaceutical form and strength, as appropriate;\n(c) quantity supplied;\n(d) name or company name and permanent address or registered place of business of the recipient;\n(e) batch number;\n(f) date of expiry.\n2. The records referred to in paragraph 1 shall be available for inspection by competent authorities for one year after the date of expiry of the batch or at least five years from recording, whichever is longer.",
  "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/96",
    "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."
}