Healthcare & Medical Devices: Developing a Comprehensive Development Plan

The Program Capacity Buildingprogram, 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, among other topics:

• MDR classification (I–III) and CE marking;
• the ISO 13485 standard;
• 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 writing to Please specify your position and department.

To learn about all the modules offered by the program, see the complete Capacity Building course catalog.