Medical Devices: From Design to Marketing (DMCC)

The objectives of the program are to provide students with knowledge and skills covering all stages of the medical device life cycle (from design to marketing)

To train professionals specializing in the design, evaluation, production, and regulation of medical devices by developing students’ ability to adapt to the scientific, industrial, and societal environment through a work-study program and interactive learning methods.

Ability to design a medical device based on scientific and technical principles related to biomaterials,

 Gain expertise in the various areas of the medical device industry throughout its lifecycle within the company (R&D, Production, Regulatory Affairs, Quality, Marketing, etc.).

• Design projects in compliance with international regulations; establish the conditions and controls necessary to ensure quality, from the design through to the marketing of medical devices;
• Establish and maintain all documentation subject to inspection by international health authorities.
• Analyze the current situation and identify the factors driving change that lead to innovation.
• Study and determine the procedures to be followed for each manufacturing process—Compile the CE marking documentation.
• Understand and master the various stages of medical device design. Develop specifications for an application. Compile a design dossier. Understand the regulatory framework governing health products and their design.
• Analyze the scientific, medical, and economic value of a new medical device based on the state of the art (scientific articles, patents, commercialization strategies, etc.) and taking into account production costs and returns.