+Article 38 2
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Article 38 2
2. The information sheet referred to in paragraph 1 shall specify:
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(a)
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the identity, registered trade name or registered trademark, and contact details of the manufacturer and, where applicable, of its authorised representative;
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(b)
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the name and version of the EHR system and date of its release;
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(c)
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the intended purpose of the EHR system;
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(d)
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the categories of electronic health data that the EHR system has been designed to process;
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(e)
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the standards, formats and specifications supported by the EHR system and versions of those standards, formats and specifications.
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1. Pārskats
1.1 Atsauces
1.2 Identificētās prasības
1.3 Saistītie standarti
2. Identificētās prasības
3. Saistītie standarti
- Builddate: 05.03.2025 00:00:00 -Doknr: CELEX:32025R0327
- EULAW -
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DE: Rechtsakte der Europäischen Union aus EUR-Lex, https://eur-lex.europa.eu/. © Europäische Union. Weiterverwendung nach Beschluss 2011/833/EU mit Quellenangabe gestattet; die konsolidierten Fassungen stehen unter CC BY 4.0 (Rechtlicher Hinweis von EUR-Lex). In Abschnitte aufgeteilt und in das GRCA-Format umgewandelt, der Wortlaut unverändert. Verbindlich sind allein die im Amtsblatt der Europäischen Union veröffentlichten Rechtsakte.
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