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NEOMED Services was founded by 4 associates, with complementary skills, who have the willingness to guide medical device manufacturers in design, validation and regulation issues. Thanks to their experience, they have developed an organization and a methodology specially adapted to the requirements of medical devices. NEOMED Services provides you with a customized support for the success of your project. 


Julien has acquired 13 years experience in the development of medical devices, whether in the field of Research and Development (CAD, search solutions, project management) or in the field of documentary (CE marking file, risk management record, etc.). With his knowledge of textile and flexible materials and his skills, he now has a broad vision of the development of a medical device and can intervene in many issues throughout the projects.


Regulatory and Clinical Affairs Manager
Sébastien is graduated in biology with a specialization in clinical evaluation and regulatory affairs. With his 10 years of experience in medical devices and his significant involvement in Research and Development, Sebastien knows how to act early on the conception process. His knowledge and skills also comes into action to edit regulatory documents (clinical evaluation file, risk management file, etc.).


Industrialization & Process Validation Engineer
Jérémy who graduated in Mechanical Engineering from the INSA, applies his industrialization expertise to the medical devices. During 7 years, he was in charge of the industrialization and validation of equipments and processes used in a production line. He has also developed skills in the design of special machines (CAD, specification drafting, solution finding) in order to meet customer needs


Regulatory and Clinical Affairs Officer 
With her background in biology and crop production, Mylène has acquired during her 6 years of experience a scientific rigor and an analytical skill in records of medical devices for export. These various transversal skills allowed her to join the NEOMED Services team.
In collaboration with Sébastien and Léonore, Mylène is in charge of regulatory and clinical affairs.


Regulatory and Clinical Affairs Officer 
After a Master 2 specialized in medical devices and biomaterials, Léonore has joined NEOMED Services to assist Sébastien in the writing of clinical evaluation files but also on regulatory procedures.


Business Developer
Vincent is currently in Master 2 in Business Engineering, specializing in the commercial development of the healthcare industry.
He joined NEOMED Services to be in charge of the business Development

NEOMED Services
ZI Douai-Dorignies
Rue Becquerel
59500 DOUAI

Phone : +33 3 27 94 41 13