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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

OpenOpen reading. No metering is planned for this class.

EHDSOffisiell kilde

Hva siden er
Agent, EHDS artikel 30
Lest mot offisiell kilde
2026-08-31Fersk
Ansvarlig utgiver
ExploreWorld Legal, redaksjonenAnsvarsposisjon

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

  1. Hvis: alla(in_scope = true, punkt = 1)

    Paragraph 1 applies

    1. Manufacturers of EHR systems shall:

    Punkt 1

  2. Hvis: alla(in_scope = true, punkt = 2)

    Paragraph 2 applies

    (a)

    Punkt 2

  3. 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

  4. Hvis: alla(in_scope = true, punkt = 4)

    Paragraph 4 applies

    (b)

    Punkt 4

  5. 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

  6. Hvis: alla(in_scope = true, punkt = 6)

    Paragraph 6 applies

    (c)

    Punkt 6

  7. 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

  8. Hvis: alla(in_scope = true, punkt = 8)

    Paragraph 8 applies

    (d)

    Punkt 8

  9. 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

  10. Hvis: alla(in_scope = true, punkt = 10)

    Paragraph 10 applies

    (e)

    Punkt 10

  11. Hvis: alla(in_scope = true, punkt = 11)

    Paragraph 11 applies

    draw up the EU declaration of conformity in accordance with Article 39;

    Punkt 11

  12. Hvis: alla(in_scope = true, punkt = 12)

    Paragraph 12 applies

    (f)

    Punkt 12

  13. Hvis: alla(in_scope = true, punkt = 13)

    Paragraph 13 applies

    affix the CE marking of conformity in accordance with Article 41;

    Punkt 13

  14. 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

  1. 11. Manufacturers of EHR systems shall:
  2. 2(a)
  3. 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. 4(b)
  5. 5ensure that the harmonised software components of their EHR systems are not adversely affected by other software components of the same EHR system;
  6. 6(c)
  7. 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. 8(d)
  9. 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. 10(e)
  11. 11draw up the EU declaration of conformity in accordance with Article 39;
  12. 12(f)
  13. 13affix the CE marking of conformity in accordance with Article 41;
  14. 14(g)

Opphav

treatyTFEU art. 288 (förordning)
act32025R0327
chapter
article30
paragraphs14
jurisdictionEuropean Union (EU)
supervisor
national

Grensesnitt

callhttps://legal.exploreworldai.com/api/public/v1/agents/helsodata-2025-327-30/run
methodGET
outputmatched, outcome, trace, missing, hash
Kvote60 anrop per minut och adress, utan nyckel
stabilityRegelträdet versioneras. En ändring byter artefakthash, aldrig adress.

Hasher

textsha256:4027a9d10e7e626c6f0eaa7ba19dfac6c37b0b554f74559c5412cd5d93166126
scriptsha256:3f8584a0b83765c9a71b56bc6c6c69f9ea0fc6290c2d4ea870b82b96b2c5bfda
enginesha256:0a4bd50d21f8ec9be383fc091511008b76ad61909cbfb674eab56fe567fbd7a0
agentsha256:d324f494b153188648d6a1a25b4a51132e321e789b1c6c8d138bace05138b141
versionagent-engine-1+legal-2026-08-25 / d324f494b1531886

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).