When Are LLMs for Clinical Documentation Considered Medical Devices Under the European Medical Device Regulation (MDR)?. TEST BioLaw Journal - Rivista di BioDiritto, [S. l.], n. 4, p. 315–341, 2026. DOI: 10.15168/2284-4503-3927. Disponível em: https://teseo-ojs35-test.archicoop.it/biolaw/article/view/3927. Acesso em: 7 jul. 2026.