Services

Each device has its own innovation and sometimes innovative therapeutic act associated. These products require the development of an appropriate strategy based on the analysis of solid scientific evidence. Why AD- DM Consulting with you to gather the necessary elements to a front-line position in the target market .

Indeed prove the effectiveness of a health technology requires the value of clinical data, the support and vision of Key opinion leaders, the public affairs management and a clear understanding of the reimbursement process of the European market.

In addition, the assessment of the medical device efficiency (ratio cost / effectiveness) is now an essential step in the public health assessment process.

AD- DM Consulting assists your company in the regulatory and quality affairs to obtain the CE mark, in the implementation of clinical investigation (clinical study, literature) and economic value to develop the European market access strategy and reimbursement process.

 

CE Mark and Quality Standard

marquage-CE

Clinical Strategy

strategie-clinique

Market Access – Reimbursement / Pricing

remboursement

Regulatory Affairs

conseil-reglementaire

Public Affairs & Lobbying

lobbying

Communication Strategy

conseil-communication