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Healthcare

AI compliance for healthcare.
Patient data, clinical AI, diagnostic support — provable and protected.

Healthcare organizations deploying GenAI for diagnostic support, clinical documentation, or patient triage operate under GDPR, the EU AI Act, and sector-specific regulations. Patient data is special-category data under GDPR. High-risk AI systems under the EU AI Act require continuous oversight evidence. We help you deploy AI safely — and prove it to regulators, patients, and medical boards.

The challenge

AI systems processing patient data for diagnosis, treatment recommendation, or triage are classified as high-risk under the EU AI Act. GDPR Article 9 imposes strict conditions on health data processing. Every AI-assisted clinical decision must leave a trail — who was involved, what data was used, how the AI contributed, and how the clinician reviewed it.

How we work

1

Maturity

2

Strategy

3

Pilot

4

Proof

01

Maturity assessment

We audit your AI deployment landscape — diagnostic support, clinical documentation, patient triage — against EU AI Act Art. 14, GDPR Art. 9, and national health data regulations. One-week assessment with compliance gap analysis.

02

Strategy & architecture

We design a compliance architecture for healthcare AI. Data protection impact assessment (DPIA) framework, patient consent workflows, human oversight documentation, special-category data safeguards.

03

Pilot deployment

We deploy RADAR with a controlled clinical AI workflow, capturing every decision, every data access, every clinician review as structured, chain-verified evidence.

04

Regulatory proof

GDPR Art. 9 processing records. EU AI Act Art. 14 human oversight evidence. National health authority documentation. All verifiable by your DPO and external auditors.

Where RADAR fits

Every AI-assisted clinical decision involves special-category data and high-risk classification. RADAR captures, hashes, and seals each interaction — creating the evidence layer that satisfies GDPR, the EU AI Act, and medical board scrutiny.

Let's scope your engagement.

We start with a free 30-minute call to understand your clinical AI use cases, your data protection framework, and your regulatory timeline. No commitment.

Book a scoping call