{
  "url": "https://openlegislation.uk/eu-regulation-2013-354/annex/title-1/section-2",
  "json_url": "https://openlegislation.uk/eu-regulation-2013-354/annex/title-1/section-2.json",
  "legislation": "eur/2013/354",
  "legislation_title": "Commission Implementing Regulation (EU) No 354/2013 of 18 April 2013 on changes of biocidal products authorised in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2013-354",
  "path": "annex/title/1/section/2",
  "kind": "section",
  "number": "2",
  "heading": "Administrative changes of products which can be notified after implementation",
  "text": "An administrative change of a product which can be notified after implementation is an administrative change, the knowledge of which is not important for purposes of control and enforcement. Such changes include those listed in the following table, provided that the conditions therein are met:\nOJ L 353, 31.12.2008, p. 1.\nAuthorisation holder\n1.\nChange in other administrative details of the authorisation holder than the name and address.\nFormulator(s) of the biocidal product\n2.\nChange in the name, the administrative details or the formulating location of the biocidal product formulator, where the biocidal product composition and the formulating process remain unchanged.\n3.\nDeletion of a formulating location or a formulator of the biocidal product\n4.\nAddition of a formulator of the biocidal product, where the biocidal product composition and the formulating process remain unchanged.\nManufacturer(s) of the active substance(s)\n5.\nChange in the name or the administrative details of a manufacturer of the active substance, where the manufacturing location and process remain unchanged and the manufacturer remains listed in accordance with Article 95(2) of Regulation (EU) No 528/2012\n6.\nDeletion of a manufacturer or a manufacturing location of the active substance\nConditions of use\n7.\nMore precise instructions for use, where only wording but not content of instructions are changed.\n8.\nRemoval of a particular claim, such as a specific target organism or a specific use.\n9.\nRemoval of a category of users.\n10.\nAddition, replacement or modification of a measuring or administration device not relevant for the risk assessment and not regarded as a risk mitigation measure.\nClassification and labelling\n11.\nChange to the classification and labelling, where the change is limited to what is necessary to comply with newly applicable requirements of Regulation (EC) No 1272/2008 of the European Parliament and of the Council.",
  "extent": "E+W+S+N.I.",
  "status": null,
  "version": "current",
  "annotations": [
    {
      "type": "footnote",
      "label": "f1",
      "text": "OJ L 353, 31.12.2008, p. 1."
    }
  ],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eur/2013/354/annex/title/1/section/2",
    "retrieved_at": "2026-11-01T14:48:43.181490+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."
}