Healthcare & medical devices training: structuring a comprehensive development plan

The program Capacity Buildingprogram, led by the University Innovation Cluster at the University of Montpellier, offers targeted training in innovation and research promotion. Through thematic modules led by experts, it supports the development of skills among professionals involved in innovative projects.

On June 11, a training session will be devoted to the regulatory, technical, and financial development of a medical or digital device. It is intended for personnel involved in healthcare projects that require a thorough understanding of the requirements applicable to medical devices.

This session will cover the following topics:

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

Are you interested in this training? Let us know by writing to specifying your position and organization.

To discover all the modules offered by the program, consult the complete Capacity Building training catalog.