Healthcare and Medical Devices Training: Developing a Comprehensive Development Plan

The Program Capacity Building, led by the University Innovation Hub at the University of Montpellier, offers targeted training in innovation and research commercialization. Through thematic modules led by experts, it supports the professional development of professionals involved in innovative projects.

On June 11, a training session will focus on the regulatory, technical, and financial aspects of developing a medical or digital device. It is intended for staff involved in healthcare projects that require a thorough understanding of the requirements applicable to medical devices.

This session will cover the following topics:

• MDR classification (Class I to III) and CE marking;
• ISO 13485;
• TRL matrices and clinical studies;
• technical documentation;
• funding programs (EIC, Bpifrance, Europe);
• practical examples of project structuring.

Are you interested in this training course? Let us know by emailing please specify your position and department.

To explore all the modules offered by the program, please consult the complete Capacity Building course catalog.