This paper is in the following e-collection/theme issue:

Tutorial (81) Clinical Information and Decision Making (1993) Digital Health Reporting Standards, Quality and Transparency in e-Research (140) Artificial Intelligence (2239) Standards and Interoperability (143) AI Governance and Policy (23)

Published on in Vol 27 (2025)

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/81184, first published .
AI Act Compliance Within the MyHealth@EU Framework: Tutorial

AI Act Compliance Within the MyHealth@EU Framework: Tutorial

AI Act Compliance Within the MyHealth@EU Framework: Tutorial

Authors of this article:

Monika Simjanoska Misheva1 Author Orcid Image ;   Dragan Shahpaski2 Author Orcid Image ;   Jovana Dobreva1 Author Orcid Image ;   Djansel Bukovec3 Author Orcid Image ;   Blagojche Gjorgjioski4 Author Orcid Image ;   Marjan Nikolov2 Author Orcid Image ;   Dalibor Frtunikj2 Author Orcid Image ;   Petre Lameski1 Author Orcid Image ;   Azir Aliu5 Author Orcid Image ;   Kostadin Mishev1 Author Orcid Image ;   Matjaž Gams6 Author Orcid Image
Article Authors Cited by (2) Tweetations (3) Metrics

Journals

  1. Vichentijevikj I, Mishev K, Simjanoska Misheva M, Yamanishi Y. Prompt-to-Pill: Multi-Agent Drug Discovery and Clinical Simulation Pipeline. Bioinformatics Advances 2026;6(1) View
  2. Lima V, Mozini M, Alves D. Second-Opinion Systems for Rare Diseases: A Scoping Review of Digital Workflows and Networks. Informatics 2026;13(1):6 View