ECTS
120 credits
Duration
2 years
Training structure
Faculty of Pharmacy
Language(s) of instruction
French
Presentation
The DMCC program is a cross-disciplinary and multi-disciplinary program that provides in-depth knowledge of the medical device sector.
100% success rate in 2021-2022 exams
Success rate
Objectives
The objectives of the course are to provide students with knowledge and skills on all stages of the medical device life cycle (from design to marketing)
To train managers 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 sandwich course and interactive learning methods.
Know-how and skills
Ability to design a medical device from scientific and technical bases on biomaterials,
Master the specialties of the medical device throughout its life cycle in the company (R&D, Production, Regulations, Quality, Marketing...).
- To design projects in compliance with international regulations, to put in place the conditions and controls to ensure quality, from design to marketing of medical devices;
- Establish and maintain all documentation inspectable by the International Health Authorities.
- Analyze the existing situation and determine the parameters of evolution leading to innovation.
- To study and determine the procedures to be followed for each manufacture - To constitute the files of CE marking
- Master and understand the different stages of design of a medical device. Establish the specifications of an application. To constitute a design file. To situate health products and their design in their regulatory framework.
- Analyze the scientific, medical and economic interest of a new medical device according to the state of the art (scientific article, patent, methods of valorization...), according to production costs and yields).
Organization
Open in alternation
Type of contract | Apprenticeship contract, Professionalization contract |
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According to the provisional calendar provided by the course.
Internships, tutored projects
Internship | Mandatory |
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Duration of the course | Master 1: 3 to 5 months / Master 2: 4 to 6 months |
Internship abroad | Possible |
Tutored project which consists in building the path of a DM (in group of 4 supervised by an industrialist)
Program
Students in the DMCC track receive training based on two complementary axes:
1- Acquisition of knowledge obtained from courses given by professionals in the DM sector [designers (academic and industrial researchers and engineers)], users (doctors, surgeons, pharmacists, etc.), institutions (ANSM, notified body, HAS, etc.) and industrialists (development, production, regulations, evaluation, quality, marketing)].
2- DM life cycle project aiming to build the progressive path of a DM that leads from conception to marketing
Select a program
Master 1 Medical devices: from design to marketing
Master 1 Medical devices: from design to marketing
Databases - Epidemiology and health environment
5 creditsStrat de Dvpmt prodts de santé - Gestion de prjt et dvpmt clin
5 creditsElective courses Semester 1
5 creditsYour choice: 1 of 4
Regulatory and financial aspects, Quality and safety TC
5 creditsBiotechnologies applied to health
5 creditsModern languages and communication
5 creditsEnglish Semester 1
Modern languages
Choice of 1 of 3
Spanish Semester 1
2.5 creditsGerman Semester 1
2.5 creditsOther language Semester 1
2.5 credits
Documentation and communication
Internship in a company
10 creditsProject-based learning
5 creditsEnglish and 2nd language
5 creditsEnglish Semester 2
2.5 creditsModern languages Choice 2
2.5 creditsChoice of 1 of 3
Medical device concept° strategy and fields of application
5 creditsShaping and using biomaterials in healthcare
5 credits
Master 2 Medical devices: from design to marketing
Master 2 Medical devices: from design to marketing
And then
Further studies
Continuation in Doctorate possible
Professional integration
Opportunities in the medical device sector (R&D, Industrialization, Quality, Regulation, Pre-clinical and clinical evaluation, Marketing)
- Research and Development Engineer.
- Technical sales engineers.
- Responsible for the production planning of medical devices.
- Quality and regulatory affairs manager.
- Project manager in R§D.
- Industrial development manager.