+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. Apžvalga
| Pavadinimas |
Reguliavimas |
,
1.1 Nuorodos
1.2 Nustatyti reikalavimai
1.3 Susiję standartai
2. Nustatyti reikalavimai
Reikalavimai
| Šaltinis |
Reikalavimas |
3. Susiję standartai
Standartai
| Šaltinis |
Reikalavimas |
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