Strategic analysis and market access roadmap
- Position the technology in the therapeutic and competitive environment;
- Identify missing data according to clinical development level;
- Analyze the market on public data: SNIIRAM and PMSI;
- Organize and manage expert boards or practice surveys;
- Evaluate device eligibility for the various financing pathways:
- Common law: LPPR, intra-DRG (GHS), technical procedures (NABM and CCAM), technical packages;
- Innovation financing: RIHN, Forfait Innovation, Ministerial Research Programs, Article 51 and BPI Funding;
- Telemonitoring.
- Keep a watch on regulatory and scientific aspects of the concerned therapeutic area;
- Organize and support strategic meetings with authorities.
More activities on Market Access
For all health products
Medical devices (DM)
- Single use, implantable, capital equipment, etc
- Therapeutic, Diagnostic or prognostic
In vitro diagnostic devices
- Biological procedure acts,
- Companion tests,
- Capital equipment and consumables
And other innovative technologies
- Connected medical devices or tele surveillance activities,
- Foods for special medical purposes
- …