Free AI Act diagnostic : identify your obligations in 3 minutes
Identify in a few minutes your role under the European Artificial Intelligence Regulation (EU) 2024/1689, classify your AI system's risk level, and discover your regulatory obligations. Completely free and no registration required.
Free, no registration required
Under 3 minutes
Smart questionnaire of 8-10 questions tailored to your situation
100% free
No commitment, no credit card, accessible without registration
Personalized report
Detailed obligations with references to Regulation articles
Official text compliant
Based on Regulation (EU) 2024/1689 and AI Office guidelines
Two paths based on your situation
Whether you simply use AI tools or develop your own systems, we have the right diagnostic for you.
What is the AI Act diagnostic?
Regulation (EU) 2024/1689, commonly known as the AI Act, is the world's first comprehensive legal framework regulating artificial intelligence. It imposes different obligations depending on your role in the AI value chain and your system's risk level.
Our automated diagnostic analyzes your situation in a few questions to provide you with:
- Your legal qualification (provider, deployer, importer, distributor)
- Your system's risk classification (prohibited, high, limited, minimal)
- The list of your obligations with references to applicable articles
- The application timeline that concerns you
Roles identified by the diagnostic
Provider
You develop or market an AI system
Deployer
You use an AI system in your activity
Importer / Distributor
You import or distribute AI systems
Risk levels under the AI Act
The Regulation classifies AI systems into four risk categories, each with specific obligations.
Ready to assess your AI system?
Answer a few questions to identify your role, classify your risk level and discover your obligations under the AI Act.
Free, no registration required
Why perform an AI Act diagnostic?
A regulation with multiple deadlines
The AI Act applies progressively between 2024 and 2028. Prohibited practices have applied since February 2025, GPAI rules since August 2025, and transparency obligations since 2 August 2026. High-risk systems are scheduled for December 2027 and regulated products for August 2028.
Identifying your situation now allows you to anticipate your obligations and plan your compliance.
Significant sanctions
Non-compliance with the Regulation exposes you to fines of up to 35 million euros or 7% of annual global turnover for prohibited practices, 15 million or 3% for other violations.
An early diagnostic helps you identify risks and prioritize your compliance actions.
Turn your diagnostic into an action plan
Explore the deliverables that match the role and risk level identified by your assessment.
Annex IV technical documentation
Structure the evidence required by Article 11 for a high-risk AI system.
Explore document generationFundamental rights impact assessment
Understand when the Article 27 fundamental rights impact assessment applies.
Read Article 27GPAI model documentation
Identify the documentation duties of general-purpose AI model providers.
Read Article 53Frequently asked questions about the AI Act diagnostic
Everything you need to know before launching your compliance diagnostic under the European Regulation on artificial intelligence
An AI Act compliance diagnostic is a structured assessment that analyses your use of artificial intelligence under Regulation (EU) 2024/1689. It determines your role (provider, deployer, importer or distributor), classifies the risk level of your AI system (unacceptable, high, limited or minimal) and identifies the specific regulatory obligations that apply to your situation. At AiActo, this diagnostic is entirely free and takes less than 5 minutes.
Yes, the AI Act compliance diagnostic offered by AiActo is 100% free, with no commitment and accessible without registration. You immediately receive your risk classification, your role under the Regulation and the list of your obligations. To save your results, generate technical documentation or access the legal AI assistant, a free account or subscription is required.
Any organisation that develops, deploys, imports or distributes an artificial intelligence system in the European Union is affected by the AI Act. This includes SMEs using ChatGPT, automatic translation tools or image generation, as well as companies developing their own AI models. Even simple use of an AI chatbot for customer service subjects you to transparency obligations. The AiActo diagnostic allows you to clarify your situation in just a few minutes.
The AI Act establishes four risk levels for AI systems: unacceptable risk (prohibited practices such as social scoring or subliminal manipulation), high risk (systems used in recruitment, education, justice or critical infrastructure), limited risk (chatbots, deepfakes, emotion recognition systems subject to transparency obligations) and minimal risk (spam filters, video games). The AiActo diagnostic automatically determines which category your system falls into.
The AI Act applies progressively: prohibited practices and AI literacy have applied since 2 February 2025, GPAI rules since 2 August 2025, and Article 50 transparency obligations since 2 August 2026. Annex III high-risk systems are scheduled for 2 December 2027 and Annex I regulated products for 2 August 2028. Carrying out a diagnostic now helps you prepare.
The penalties under the AI Act are proportional to the severity of the infringement: up to 35 million euros or 7% of annual global turnover for prohibited practices, up to 15 million euros or 3% for non-compliance with high-risk system obligations, and up to 7.5 million euros or 1.5% for providing inaccurate information to authorities. Reduced caps apply for SMEs and start-ups. The AiActo diagnostic helps you identify your risks before these deadlines.
The quick SME diagnostic (2 minutes, 5 questions) is aimed at businesses using existing AI tools (ChatGPT, automatic translation, image generation) and automatically generates a compliant transparency document. The full diagnostic (5 minutes, in-depth analysis) is designed for organisations developing or integrating AI systems into their products: it provides a detailed risk classification, identification of your regulatory role and a personalised action plan with applicable articles.
AiActo guarantees maximum protection of your data. Hosting is 100% European (Scaleway, France), in full compliance with GDPR. Your diagnostic responses are never shared with third parties. The diagnostic without registration does not retain any personal data. If you create an account, your data is encrypted and you can export or delete it at any time in accordance with your GDPR rights.