Agent · helsodata-2025-327-30
EHDS artikel 30: Obligations of manufacturers of EHR systems
Strukturelt tre: artikkelens egne punkter, ordrett.
CELEX 32025R0327 · 2026-08-31 · Vekt 70 · minimal-risk
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- Hva siden er
- Agent, EHDS artikel 30
- Lest mot offisiell kilde
- 2026-08-31Fersk
- Ansvarlig utgiver
- ExploreWorld Legal, redaksjonenAnsvarsposisjon
Kort svar
What does EHDS Article 30 require, and what outcome does the rule tree give?
EHDS Article 30 is tested here by a deterministic rule tree of 14 rules, built from the article's own conditions. The tree reads your facts and names the outcome that applies, starting with Paragraph 1 applies, carrying paragraph citation, content hash and read date 2026-08-31 against CELEX 32025R0327. The outcome is a machine classification, not a compliance decision.
EHDS Article 30Lest mot utgiveren 2026-08-31Offisiell tekst
- Paragraph 1 applies. 1. Manufacturers of EHR systems shall:
- Paragraph 2 applies. (a)
- Paragraph 3 applies. ensure that the harmonised software components of their EHR systems and the EHR systems themselves, to the extent that this Chapter establishes requirements for them, are in conformity with the essential requirements laid down in Annex II and with the common specifications in accordance with Article 36;
En kildehenvisning, ikke juridisk rådgivning.
Jurisdiksjon
Samme agent, lest med ett lands øyne.
Inndata
- in_scopeThe article applies to the situationboolean
- punktParagraph of the articleenum (1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14)
Regeltre
Hvis: alla(in_scope = true, punkt = 1)
Paragraph 1 applies
1. Manufacturers of EHR systems shall:
Punkt 1
Hvis: alla(in_scope = true, punkt = 2)
Paragraph 2 applies
(a)
Punkt 2
Hvis: alla(in_scope = true, punkt = 3)
Paragraph 3 applies
ensure that the harmonised software components of their EHR systems and the EHR systems themselves, to the extent that this Chapter establishes requirements for them, are in conformity with the essential requirements laid down in Annex II and with the common specifications in accordance with Article 36;
Punkt 3
Hvis: alla(in_scope = true, punkt = 4)
Paragraph 4 applies
(b)
Punkt 4
Hvis: alla(in_scope = true, punkt = 5)
Paragraph 5 applies
ensure that the harmonised software components of their EHR systems are not adversely affected by other software components of the same EHR system;
Punkt 5
Hvis: alla(in_scope = true, punkt = 6)
Paragraph 6 applies
(c)
Punkt 6
Hvis: alla(in_scope = true, punkt = 7)
Paragraph 7 applies
draw up the technical documentation of their EHR systems in accordance with Article 37 before placing those EHR systems on the market, and subsequently keep it up to date;
Punkt 7
Hvis: alla(in_scope = true, punkt = 8)
Paragraph 8 applies
(d)
Punkt 8
Hvis: alla(in_scope = true, punkt = 9)
Paragraph 9 applies
ensure that their EHR systems are accompanied, free of charge for the user, by the information sheet provided for in Article 38 and clear and complete instructions for use;
Punkt 9
Hvis: alla(in_scope = true, punkt = 10)
Paragraph 10 applies
(e)
Punkt 10
Hvis: alla(in_scope = true, punkt = 11)
Paragraph 11 applies
draw up the EU declaration of conformity in accordance with Article 39;
Punkt 11
Hvis: alla(in_scope = true, punkt = 12)
Paragraph 12 applies
(f)
Punkt 12
Hvis: alla(in_scope = true, punkt = 13)
Paragraph 13 applies
affix the CE marking of conformity in accordance with Article 41;
Punkt 13
Hvis: alla(in_scope = true, punkt = 14)
Paragraph 14 applies
(g)
Punkt 14
Hvis ingen regel treffer: The article is not stated to apply, or no paragraph is selected. The agent abstains rather than guesses.
Artikkelteksten som ble lest
- 11. Manufacturers of EHR systems shall:
- 2(a)
- 3ensure that the harmonised software components of their EHR systems and the EHR systems themselves, to the extent that this Chapter establishes requirements for them, are in conformity with the essential requirements laid down in Annex II and with the common specifications in accordance with Article 36;
- 4(b)
- 5ensure that the harmonised software components of their EHR systems are not adversely affected by other software components of the same EHR system;
- 6(c)
- 7draw up the technical documentation of their EHR systems in accordance with Article 37 before placing those EHR systems on the market, and subsequently keep it up to date;
- 8(d)
- 9ensure that their EHR systems are accompanied, free of charge for the user, by the information sheet provided for in Article 38 and clear and complete instructions for use;
- 10(e)
- 11draw up the EU declaration of conformity in accordance with Article 39;
- 12(f)
- 13affix the CE marking of conformity in accordance with Article 41;
- 14(g)
Opphav
Grensesnitt
Hasher
Artefakter
Ingen rådgivning. Deterministisk regeluppslagning. Ingen juridisk rådgivning, inget efterlevnadsbeslut, ingen bedömning av ett enskilt ärende.
Sitering: 32025R0327 art. 30, Obligations of manufacturers of EHR systems. ExploreWorld Legal, https://legal.exploreworldai.com/agent/helsodata-2025-327/artikel-30 (hämtad 2026-08-31, bevis sha256:29d20540c27ceae6, bygge legal-2026-08-25).