The problem you're facing
Reports, letters, records: administrative time encroaches on care time. Consumer AI tools are unusable in healthcare : personal data sent outside Europe, unverifiable answers, no traceability.
Our answer
We build healthcare AI solutions with the sector's constraints as the starting point: data hosted in Europe, minimisation, complete traceability and human validation on any clinically relevant content.
What LaMeDuSe AI takes care of
- Document automation: letters, reports
- Pre-filling under professional supervision
- File summarisation with source references
- European hosting and documented GDPR compliance
- Complete access and processing traceability
- Integration with your existing information system
- Team training on governed usage
Our methodology
- 1
Understanding sector constraints
Compliance, confidentiality, regulation: constraints dictate the technical architecture from scoping.
- 2
Prioritised use case
Start with the highest-gain process, with before/after measurement.
- 3
Integration with the existing
Connection to sector tools (clinical systems, case managers, ERP) rather than a parallel system.
- 4
Documented compliance
Traceability, minimisation and evidence for your audits and processing records.
Technologies
Security & compliance
European hosting by default, encryption, data minimisation and access traceability : GDPR and sector-aligned.
Hosting
Group datacenters in France, Germany and Switzerland; full self-hosting option for regulated data.
Maintenance
Compliance tracking through changes, periodic security reviews and support by the team that knows your sector.
Why LaMeDuSe AI
The LaMeDuSe group already hosts healthcare data on its European infrastructure: confidentiality isn't a marketing promise, it's the group's architecture.
Frequently asked questions
In our French, German or Swiss datacenters, with encryption, access traceability and minimisation. For the strongest requirements, full self-hosting, including the AI models, eliminates any external sending.
No, and we don't propose that: AI prepares, summarises and pre-fills, but every clinically relevant piece goes through professional validation. The tool saves administrative time; it doesn't diagnose.
Yes: structural compliance (minimisation, encryption, traceability), signed DPA, and evidence for your processing records. Your country's regulatory specifics are scoped at the start.
We connect to your existing information system rather than imposing a parallel tool. Interfaces depend on your software; the integration analysis is part of scoping.