Samtykke fra patienter
Retsgrundlag for behandling
Sektion kaldt “Retsgrundlag for behandling”Samtykke (GDPR Art. 9(2)(a)): Hvis optagelser og AI bruges til formål udover direkte patientbehandling, skal der indhentes et udtrykkeligt samtykke.
Retlig forpligtelse (GDPR Art. 9(2)(b)): Hvis optagelser og AI er en integreret del af dokumentationsprocessen og dermed nødvendig for at opfylde sundhedsretlige krav til journalføring, kan behandlingen ske uden særskilt samtykke.
Dermloop software does not perform medical analysis or provide diagnostic output. Clinical evaluation is performed by qualified healthcare professionals. Seranote is a documentation assistant; all clinical content in generated notes must be reviewed and approved by the treating clinician before use. The dermoscope integrated in the Dermkit system pack is a CE-marked Class I medical device manufactured by a third party and supplied as part of the Dermkit MDR Article 22 system pack.