{
  "url": "https://openlegislation.uk/eu-regulation-2013-284/annex/part-B/division-5/division-1",
  "json_url": "https://openlegislation.uk/eu-regulation-2013-284/annex/part-B/division-5/division-1.json",
  "legislation": "eur/2013/284",
  "legislation_title": "Commission Regulation (EU) No 284/2013 of 1 March 2013 setting out the data requirements for plant protection products, in accordance with Regulation (EC) No 1107/2009 of the European Parliament and of the Council concerning the placing of plant protection products on the market (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2013-284",
  "path": "annex/part/B/division/5/division/1",
  "kind": "division",
  "number": null,
  "heading": "Introduction",
  "text": "The provisions of this Section only cover analytical methods required for post-registration control and monitoring purposes.\nIt is desirable to have a plant protection product without contaminants, if possible. The level of acceptable contaminants shall be judged from a risk assessment point of view, by the competent authority.\nBoth production and product must be subject to a continuous quality control by the applicant. The quality criteria for the product shall be submitted.\nFor analytical methods used for generation of data as required in this Regulation or for other purposes the applicant has to provide a justification for the method used; where necessary separate guidance will be developed for such methods on the basis of the same requirements as defined for methods for post-registration control and monitoring purposes.\nDescriptions of methods must be provided and include details of equipment, materials and conditions used. The applicability of existing CIPAC methods must be reported.\nAs far as practicable these methods must employ the simplest approach, involve the minimum cost, and require commonly available equipment.\nFor this Section the following applies:\nImpurities, metabolites, relevant metabolites, residues\nAs defined in Article 3 of Regulation (EC) No 1107/2009\nRelevant impurities\nImpurities, as defined above, that are of concern for human or animal health and/or the environment\nOn request the following samples must be provided:\n(i)samples of the preparation;\n(ii)samples of the micro-organism as manufactured;\n(iii)analytical standards of the pure micro-organism;\n(iv)analytical standards of relevant metabolites and all other components included in the residue definition;\n(v)if available, samples of reference substances for the relevant impurities.",
  "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/2013/284/annex/part/B/division/5/division/1",
    "retrieved_at": "2026-11-01T14:48:45.647621+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."
}