AI Act (NL) Recital 147 NL
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Recital 147 — toegang testfaciliteiten conformiteitsbeoordeling

Conformity Assessment for AI Systems Provider Obligations for AI Systems Healthcare
In force — consolidated2026-07-27 · CELEX 02024R1689-20260727 · ELI ↗
Version history 2
  • 2026-07-27in force CELEX 02024R1689-20260727
  • 2024-07-12 CELEX 02024R1689-20240712

Het is passend dat de Commissie voor zover mogelijk de toegang tot test- en experimenteerfaciliteiten vergemakkelijkt voor instanties, groepen of laboratoria die overeenkomstig relevante harmonisatiewetgeving van de Unie zijn opgericht of erkend en die taken uitvoeren in het kader van de conformiteitsbeoordeling van producten of apparaten die onder die harmonisatiewetgeving van de Unie vallen. Dit is met name het geval voor deskundigenpanels, deskundige laboratoria en referentielaboratoria op het gebied van medische hulpmiddelen overeenkomstig de Verordeningen (EU) 2017/745 en (EU) 2017/746.

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