ThinkLocAI - Self-hosted Enterprise AI Infrastructure
ThinkLocAI
TL

AI Infrastructure for Secure Patient Data

Process medical documentation, diagnostic analysis, and patient records without sensitive health data leaving your facility.

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Typical Problems in Healthcare

Data Privacy

Patient data is subject to the strictest privacy requirements and must not be processed externally.

Documentation Burden

Physicians often spend more time on documentation than with patients.

Information Access

Quickly finding relevant patient history in extensive medical records.

Compliance

HIPAA, GDPR, and other regulations require strict data control.

ThinkLocAI for Healthcare

Security & Compliance

Supports medical data protection requirements through fully local processing.

Document RAG

Search patient records, diagnostics, and lab reports with AI-powered analysis.

Voice Interface

Dictate findings and documentation hands-free during treatment.

Multi-User & RBAC

Ward-based access control. Physicians see different data than nursing staff.

How to Use ThinkLocAI

Clinical Documentation

Reduce documentation effort through AI-assisted text generation.

Dictate findings by voice
AI structures automatically
Suggest ICD-10 codes
Transfer to HIS

Patient History

Quick access to relevant information from extensive records.

Natural language query
Find relevant entries
Create chronological overview
Compare with normal values

Discharge Management

Automated creation of discharge letters and handover documents.

Gather stay data
Summarize diagnoses
Create medication plan
Generate discharge letter

Privacy and Compliance

Suitable for HIPAA environments

Supports US healthcare requirements

Designed for GDPR compliance

EU data protection through local architecture

On-Premise

No external data processing

Not a medical device

For documentation and research, not for diagnostics

Clinical scenarios need a separate assessment

AI-assisted triage in emergency and first-response services is classified as high-risk under the EU AI Act; those obligations apply from 2 December 2027, and from 2 August 2028 for safety components in Annex I products. Independently of that, systems intended for diagnostic or therapeutic purposes may qualify as medical devices under the MDR and therefore fall into the high-risk category via Art. 6(1). ThinkLocAI is not a medical device and is not intended for diagnosis or treatment decisions.

EU AI Act, Annex III(5)(d)

  • Define the intended purpose in writing: documentation and research rather than diagnosis
  • Clarify medical device classification with your QM and regulatory function (MDR, Art. 6(1) AI Act)
  • Anchor final clinical decision-making with the treating physician (Art. 14)
  • Align patient-related processing with professional secrecy rules and your GDPR documentation
See the full AI Act breakdown

Discuss how it fits your hospital or practice

Using clinical documentation and discharge letters as examples, we show how ThinkLocAI helps in day-to-day work.

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