IVDMD Forum

On November 16th, GMED will organize a new edition of its digital Forum dedicated to In Vitro Diagnostic Medical Devices. Follow this event live, interpreted simultaneously in English, and join our interactive exchange and debate with GMED experts, subject matter experts, and manufacturers from the IVDMD industry.

Implementation of Regulation (EU) 2017/746

Structured around interventions and roundtables from a TV studio, this forum will discuss the implementation of Regulation (EU) 2017/746 for In Vitro Diagnostic Medical Devices.

It is aimed at:

Medical device manufacturers: company managers, regulatory affairs managers, quality managers and R&D managers
Hospital buyers
Biomedical Engineers
Publishers of Mobile Health Software and Applications
Distributors and Importers of in vitro diagnostic medical devices

After each topic, dedicated chat sessions will offer the opportunity to get answers to your questions, and networking sessions will allow you to exchange with your peers.

Detailed programme and registration