Features

Two tools.
Structured compliance.

A structured audit to qualify your regulatory situation, and a document generator to produce exactly what regulators require. Built for teams who don't have time to read 144 articles of regulation.

Start free audit See pricing

Free · The audit

AI Act Audit

61 questions across 10 themes. Each answer feeds a deterministic compliance score — reproducible and defensible before a regulator. You get your risk level, your obligations and a prioritised action plan.

→Classification across the 4 AI Act risk levels
→Reproducible score — identical if nothing changed
→Obligations identified article by article
→1 free audit (first audit) · one-shot audit or document: €49

Free1 audit / 6 months

Per unit · The generator

Document generation & verification

From your audit answers, DILAIG drafts each mandatory document in legal English, structured to the regulation's exact requirements — then verifies every one: blocking fields flagged, placeholders resolved, per-article status computed.

→FRIA — Fundamental Rights Impact Assessment (Art. 27)
→EU Declaration of Conformity (Art. 47)
→Transparency notice (Art. 13 & 50)
→Technical documentation (Annex IV)
→Data Governance Plan (Art. 10)
→Post-Market Monitoring Plan (Art. 72)

49 €/ document · one-shot · included Provider

Use cases

Tailored to your situation

HR · Credit · Healthcare · Workforce

You deploy a high-risk AI system

Qualified human oversight (Art. 26)Log retention ≥ 6 monthsFRIA before deployment (Art. 27)Worker notification

Software editor · AI startup · Integrator

You build and sell an AI system

Annex IV technical documentation (Art. 11)EU Declaration of Conformity (Art. 47)Conformity assessment (Art. 43)Transparency notice (Art. 13)

DPO · Legal counsel · CTO · Consultant

You manage AI Act compliance

Structured 61-question auditScore /100 defensible before a regulatorPrioritised action plan by articleDocuments ready to review & validate

The audit, step by step

10 themes. 61 questions.
20 to 30 minutes.

Each section maps to a precise regulatory dimension of the AI Act. Here is what each step evaluates.

01AI QualificationIs your system an AI system within the meaning of Article 3? This first step decides whether the AI Act applies at all.1 q

02OrganisationIndustry, organisation size and role in the AI value chain — the parameters that define the exact scope of your obligations.3 q

03FunctioningWhat your system concretely does: its inputs, outputs and the decisions it influences. The basis of any classification.3 q

04ClassificationCross-referenced against the 8 high-risk domains of Annex III and the prohibited practices of Article 5. Sets your risk level.8 q

05DataData origin, personal data, quality measures and transfers outside the EU — the AI Act / GDPR overlap on governance.7 q

06Decision & autonomyDegree of automation, possibility of human challenge, people affected. Determines human oversight requirements (Art. 14).4 q

07Fundamental rightsImpact on vulnerable populations, discrimination risks and redress mechanisms — the foundation of the FRIA (Art. 27).3 q

08TransparencyTraceability, documentation and synthetic content. Obligations under Art. 13 & 50 — chatbots, deepfakes, generated content.5 q

09GovernanceDesignated owner, risk management, monitoring, kill switch, event logs. The most demanding block for high-risk systems.9 q

10Compliance maturityGDPR compliance, cybersecurity, AI register, AI literacy and incident reporting. Assesses your operational readiness.5 q

FAQ

Good to know

Yes. Your first full audit is free — no card required. You get your risk classification, your /100 score and the list of obligations that apply to you. To go further: one-shot audit or document at €49, or Provider subscription at €129/month.

Once your audit identifies that a Fundamental Rights Impact Assessment is required (Art. 27), the generator drafts it pre-filled with your system's context. It is then verified clause by clause and downloadable as an ODT file (compatible with LibreOffice and Word) — included in the Provider plan or €49 as a one-shot.

Yes. For providers of high-risk systems, DILAIG produces the full Annex IV technical file — design, data, performance and risk management — structured to the regulation's exact headings.

DILAIG structures and accelerates the work: a defensible score, identified obligations and ready-to-review documents. For complex or contentious cases we recommend having the output validated by your legal counsel — DILAIG gives them a complete file to work from instead of a blank page.

Your first audit
is free.

20 to 30 minutes to know exactly where you stand and what you need to prepare for the AI Act. No credit card, no commitment.

Start free audit