The Journal of Medical Device Regulation’s Editorial Advisory Board includes senior international experts in medical device and IVD regulation with extensive experience across FDA regulation, EU MDR/IVDR, UKCA compliance, software as a medical device (SaMD), clinical evaluation, quality management systems, vigilance, and post-market surveillance.
The Board supports the Journal by providing independent expert guidance on regulatory developments, editorial priorities, technical accuracy, and emerging industry trends. Members contribute through article development, topic recommendations, peer review support, and engagement with the wider international regulatory community.
Members of the Editorial Advisory Board help ensure the Journal maintains high standards of editorial quality, professional relevance, and regulatory expertise.
Haroon Atchia
Technical Director, Quality First International, London, UK
James Kuhn Jr
Regulatory Affairs Manager, ANIMAS, Chesterbrook, PA, USA (retired)
Luciano Oliveira Ferreira
Quality, Client Manager – Regulatory Services, Europe, BSI, Madrid, Spain
Principal Consultant, Co-founder and non-executive Director, Certification Body Australia
