Are you seeking assistance from Medical Device Experts?

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16 MedTech experts

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30-minute meetings

The Expert Meetings are your first step to success:

Secure a free flash meeting by sending a request on the Inova partnering platform to meet with one of our experts.

The Experts are specialised in many fields, such as:

 Regulatory affairs / Quality assurance
 Production / Sourcing
 Preclinical evaluation / Clinical affairs
 Reimbursement
 Sales and marketing strategy
 Funding and financing
 Research & development
 Merger and acquisitions
 Human resources

And many others…

How does it work? 

Each expert will have a meeting table in the Experts Area inside the exhibition space.

Please note that the number of available time slots is limited. To secure a meeting, you must book on the partnering platform beforehand.

Do not forget to request your meeting as soon as the platform opens (1 month prior to the event). Onsite meeting requests are subject to availability.

The experts: 

Mrs. Christine GRASSET
Product development, Funding innovation

10 years of experience in R&D, and the management of complex projects with various medical device and cosmetics manufacturers. Working on product development projects as a consultant, Christine oversees the quality/regulatory challenges as well as the strategies to finance innovation.

Mrs. Christine HORVAIS
HR audits, Evaluation interviews, Recruitment in Sales-Marketing-QA-RA-Clinical studies-R&D-Top management

After more than 10 years in the healthcare industry, Christine founded AXEME – a human resources company specialized in medical devices. Now since 13 years, Axeme has been recruiting talented professionals for biotech, medtech and IVD companies. Its expertise is based on listening capabilities, reactivity, and a deep understanding of the healthcare field and its associated jobs.

Mr. Cyrille MICHAUD
Quality insurance, Regulatory affairs, CE/FDA, Software medical device life cycle management

Cyrille is a consultant specialized in software medical devices, working alongside medical device manufacturers, primarily start-ups. Typical assignments are establishing the proper QA/RA strategy, setting-up a quality management system, processes relative to the life cycle of a medical software, and working on technical files for CE and FDA clearance.

Mr Eric FILION
QA/RA, FDA Clearance, MDSAP, Canada, USA, North America, Sales support

With more than 25 years of experience, Eric can help medical technology companies of any size understand rapidly the steps necessary to penetrate the North American market. With his knowledge of the many cultural and regional differences of the Canadian and US markets he can help put in place the appropriate strategy. In a short period, he can help a company understand regulatory requirements, have a better perspective of the target market, put in place the appropriate business development structure while limiting the costs associated to implementing a North American sales structure.

Mr Julien ALDEGHERI

Mr. Julien PROUTEAU
QMS ISO13485, CE-marking, Process validation

Julien assists manufacturers in the design, validation and regulation of all medical devices. From design to market launch and post-market monitoring to industrialization, Julien offers his experience and expertise throughout global projects or on specific issues.

Mrs Laura CHARBONNEL
Talent Management, Recruitment

After a first experience as an intensive care nurse, Laura became a certified business coach. She has now expertise in talent management and in jonction to her medical knowledge she understands management issues faced in the medical industry, to improve and develop talents in order to increase output.

Mr. Mathieu CHARLEUX
International business development and strategy

Mathieu  brings over 15 years of experience in international business development of medical device companies, from start-ups to well established organizations. Specialized in medical devices, his goal is to always share his experience allowing companies to rethink their business models and international business expansion strategies.

Mr. Sébastien FERRET
Clinical evaluation, Risk management, Regulatory strategy, CE-marking

Sébastien is constantly working to help insure the new medical device regulation acts on the performance and safety of medical devices, and not as a burden. Sébastien aims at sharing his experience so that the regulation fits with a company’s strategy along with the marketing message conveyed. The regulatory strategy should allow to bring proof of the performance of one’s device.

Mrs Myriam DESMET
International Expert in Regulatory, Quality and Clinical Affairs in the Medical Devices Industry

Myriam brings her expertise to start-ups and SMEs for QMS implementation & maintenance, Technical documentation, Regulatory strategy, Product registration (CE-marking, 510(k), …), Clinical strategy & management and also global strategy.

Mr. Ahmad MIHYAR
International business development and strategy

Since 2015 Ahmad has been supporting start ups, emerging and established medical device manufacturers, to expand their market presence within the Middle East and North Africa regions, covering all aspects of market analysis, Regulatory and marketing plans, our aim is to share market knowledge and experience to ensure a quick and effective market expansion.

Mrs. Blandine BOUVET
Quality management systems, trainings and audits

Biomedical engineer, with thirty-five years of professional experience in the field of in vitro diagnostic medical devices and medical devices. I work as a consultant since March 2015. Before that,  I held quality / regulatory affairs positions for manufacturers of hemostasis analyzers, medical lasers, single use sterile optical fibers, implants and ancillaries for spine surgery. All these experiences took place within an international environment. My activities are mainly related to quality management systems, trainings and audits: ISO 13485, 21 cfr 820, medical device directives (93/42/CEE and 98/79/CE) and regulations (2017/745/EU and 2017/746/EU).

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