+Article 30 4

Article 30 4

4. A manufacturer of EHR systems established outside the Union shall ensure that its authorised representative has the necessary documentation readily available in order to fulfil the tasks referred to in Article 31(2).

1. Pregled

Naslov	Regulativa

1.1 Sklici

1.2 Ugotovljene zahteve

1.3 Povezani standardi

2. Ugotovljene zahteve

Zahteve
Vir	Zahteva

3. Povezani standardi

Standardi
Vir	Zahteva

Builddate: 05.03.2025 00:00:00 -Doknr: CELEX:32025R0327
EULAW -
European Regulation published on http://eur-lex.europa.eu/