Expert Course in Medical Device (MDR) and In-Vitro Diagnostic (IVDR) Regulation. 2025-2026
Basque Health Cluster and Mondragon Unibertsitatea launch a new edition of the Expert Course in Medical Device and IVD Regulation.
Starting in January 2026, the program strengthens its content with a dedicated module on Artificial Intelligence, consolidating its position as a reference in healthcare regulatory training.
The regulatory transformation of the medical device sector has posed a major challenge for the industry in recent years, following the entry into force of the European MDR (2017/745) and IVDR (2017/746) Regulations. To address this need, Basque Health Cluster and Mondragon Unibertsitatea are launching a new edition of the Expert Course in Medical Device (MDR) and in-vitro diagnostic (IVDR) Regulation, to be held from January to July 2026.
This training program, with more than 120 teaching hours, is designed to provide professionals with the knowledge, skills, and practical tools necessary to manage the complex regulatory requirements throughout the medical device lifecycle. The course will be mainly delivered online, with live sessions, practical workshops, case studies, and personalized tutorials, along with two face-to-face sessions in Bilbao.