Findings, lab data and guidelines demand the utmost care. In this webinar, we show how diagnostics providers use AI agents: operated in Europe, with decisions you can trace.
[Date]
[Time] · 45 minutes
online and free of charge
Patient data
Critical infrastructure
Strategic company data
Research
Agents summarise lab data and previous findings. The medical decision stays with a human.
Critical: Health data is subject to special protection.
Agents compare findings with official guidelines and show relevant recommendations.
Critical: Every recommendation must be traceable to its source.
Agents check work instructions, validations and documentation for completeness.
Critical: Otherwise, gaps only come to light in the audit.
Agents answer enquiries about orders, sample status and results.
Critical: Answers must only reach authorised recipients.
Health data leaves Europe.
Requests to AI services are processed outside the EU.
Operated in Europe or on your premises.
The AI OS runs in your data centre or in a European cloud, with local models if you wish.
Recommendations without reasoning.
Nobody can trace how a result was reached.
Every step documented.
For every agent run, you can trace which data and tools were used.
Regulatory uncertainty.
It is unclear which obligations under the EU AI Act apply to an application.
A risk class for every agent.
The EU AI Act module documents the risk class, obligations and the person responsible for human oversight. Agents rated as critical do not go live.
Changes without oversight.
An agent is modified without anyone reviewing the new version.
Approval under the four-eyes principle.
New versions are tested and approved, and can be rolled back.
With patient data, this is the foundation of every AI application. In the AI OS, it is included from the first installation, at no extra cost.
A European company headquartered in Austria.
Your own data centre or a European cloud, with the same functionality.
You decide where models run, up to and including operation without external providers.
Permissions, logs and costs stay with you.
[Date]
[Time] · 45 minutes
online and free of charge
Who it is for: management, medical directors, IT and quality management at laboratories and diagnostics providers
1
AI in diagnostics: an overview of the EU AI Act, GDPR and medical device regulation
2
Critical workflows and their risks
3
Live demo: an agent with risk class, approval and log
4
Your questions
[Name]
[Role], in-manas
[Name]
[Role], medical partner
Date doesn’t suit you?
Book an initial consultation →Nothing. Taking part is free of charge.
Yes. Everyone who registers will receive the recording by email, even if they could not attend live.
No. The AI OS is the infrastructure on which applications run. Whether an application is a medical device depends on its intended purpose.
Yes. With local models, the AI OS runs entirely in your data centre.
Always a human. Agents do the preparation, and every agent has a named person responsible for human oversight.
