Market access
The process for bringing medical devices to market in France is complex.
There are numerous access pathways—whether exceptional or standard—each of which involves multiple stakeholders in the healthcare system.
Our firm provides expertise and consulting services to manufacturers seeking to bring their healthcare technologies to market, throughout the entire medical device regulatory process in France.
MedConsult’s consultants have gained extensive experience in bringing medical devices and innovative health technologies to market.
They have an impressive track record:
- strategic analyses,
- submissions of applications for the LPPR/LATM/CCAM,
- price negotiation
- and submitting applications for innovation funding (Innovation Grant, RIHN 2.0, PECAN, PECT, etc.).
All our activities
For all health products
Medical device (MD)
- Single-use, implantable, equipment, etc.
- Therapeutic, Diagnostic, or Prognostic
In vitro diagnosis
- Proceedings of Associated Biology
- Companion Test
- Equipment and supplies
And other technologies
- Connected medical devices or remote monitoring activities
- Foods for special medical purposes,
- …
