{
  "url": "https://openlegislation.uk/eu-decision-2019-1396/annex/division-4",
  "json_url": "https://openlegislation.uk/eu-decision-2019-1396/annex/division-4.json",
  "legislation": "eudn/2019/1396",
  "legislation_title": "Commission Implementing Decision (EU) 2019/1396 of 10 September 2019 laying down the rules for the application of Regulation (EU) 2017/745 of the European Parliament and of the Council as regards the designation of expert panels in the field of medical devices (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-decision-2019-1396",
  "path": "annex/division/4",
  "kind": "division",
  "number": "4",
  "heading": "For tasks referred to in Articles 55(3), 61(2), 106(10)(a) to (f) and 106(11) of Regulation (EU) 2017/745 and Article 50(3) of Regulation (EU) 2017/746, divided into categories depending on their level of complexity, the maximum number of working days is specified in Table 2.",
  "text": "Table 2\nMaximum number of working days for which experts may be remunerated for tasks under Articles 55(3), 61(2), 106(10)(a) to (f) and 106(11) of Regulation (EU) 2017/745 and Article 50(3) of Regulation (EU) 2017/746\nEach of these criteria may be applied independently\nComplexity of task (indicative criteria)\nActing as\nAllowance in full day equivalents\nCategory I — simple matter\nopinion based on examination of a low volume of data, documents and literature\nno consultation of other scientific bodies\nno information available from stakeholders including patient organisations and healthcare professionals\nindicatively, less than three months to accomplish task\nChairperson\n2\nRapporteur\n3\nCo-rapporteur\n3\nReviewing member\n0,5\nAdvisors assigned pursuant to Article 2(6) of this Decision\n1\nCategory II — complex matter\nopinion based on a significant volume of data, documents and literature\nfeedback following consultation, if any, of other scientific bodies to be examined\ninformation available from stakeholders including patient organisations and healthcare professionals, to be examined\nindicatively, three to six months to accomplish task\nChairperson\n3\nRapporteur\n5\nCo-rapporteur\n5\nReviewing member\n1\nAdvisors assigned pursuant to Article 2(6) of this Decision\n2\nCategory III — very complex matter\nopinion based on a significant volume of data, documents and literature\nhigh volume of feedback following consultation, if any, of other scientific bodies to be examined\nlarge amount of information available from stakeholders including patient organisations and healthcare professionals, to be examined\nindicatively, more than six months to accomplish task\nChairperson\n4\nRapporteur\n7\nCo-rapporteur\n7\nReviewing member\n2\nAdvisors assigned pursuant to Article 2(6) of this Decision\n2",
  "extent": "E+W+S+N.I.",
  "status": null,
  "version": "current",
  "annotations": [
    {
      "type": "footnote",
      "label": "f1",
      "text": "Each of these criteria may be applied independently"
    }
  ],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eudn/2019/1396/annex/division/4",
    "retrieved_at": "2026-11-01T15:12:35.271142+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."
}