AI Act · Regulation (EU) 2024/1689

AI Act counsel for providers and deployers

Legal advice on the EU AI Act for companies that develop, import, distribute, or use AI systems on the EU market — from role classification and risk analysis to implementation planning under the application timeline.

Fixed-fee packages available — see fees.

The AI Act attaches obligations to roles, not to technologies. The first legal question is therefore not "what does the system do?" but "who are you in the value chain, and into which risk class does the system fall?" Everything else — documentation, conformity, oversight, deadlines — follows from that answer.

01Role classification and risk class

Article 3 of the AI Act defines the four operator roles to which the regulation attaches its obligations. Which set of duties applies to your company depends on this classification — and the classification can change: a deployer that puts its name on a system, substantially modifies it, or changes its intended purpose can be re-characterised as a provider (Art. 25 AI Act).

Art. 3(3)
Provider

Develops an AI system or GPAI model, or has one developed, and places it on the market or puts it into service under its own name or trademark.

Art. 3(4)
Deployer

Uses an AI system under its own authority in a professional context — the role most companies occupy without realising it.

Art. 3(6)
Importer

Established in the EU and places on the market an AI system bearing the name or trademark of a person established outside the EU.

Art. 3(7)
Distributor

Makes an AI system available on the EU market without being its provider or importer.

High-risk classification (Art. 6, Annex III)

Whether a system is high-risk is determined by Art. 6 AI Act: either because it is a product (or the safety component of a product) covered by the EU harmonisation legislation listed in Annex I (Art. 6(1)), or because its intended use falls within one of the areas listed in Annex III — including employment and workers' management, credit scoring, education, essential private and public services, and law enforcement. The classification analysis, including the derogation in Art. 6(3) and its documentation, is the foundation of every AI Act mandate.

General-purpose AI (GPAI)

General-purpose AI models within the meaning of Art. 3(63) AI Act follow a separate track: transparency and documentation obligations under Arts. 53 et seq., and additional obligations where the model presents systemic risk (Art. 51). Companies that fine-tune or integrate third-party foundation models frequently need to determine where in this chain their own obligations begin.

02Advisory fields

Application timeline

The AI Act enters into application in stages. Since Regulation (EU) 2026/1744 (OJ 24 July 2026, in force 27 July 2026) amended Article 113 of the AI Act, four dates now structure most compliance planning:

2 August 2025
GPAI rules apply — including Art. 54 AI Act. Obligations for providers of general-purpose AI models have applied since this date.
2 August 2026
Art. 101 AI Act applies: the Commission may impose fines on providers of general-purpose AI models. The high-risk regime does not start on this date — it was deferred, see below.
2 December 2027
Chapter III, Sections 1 to 3 — including the authorised-representative duty in Art. 22 AI Act — apply to systems classified as high-risk under Art. 6(2) and Annex III. Deferred from 2 August 2026 by Regulation (EU) 2026/1744.
2 August 2028
The same rules apply to systems classified as high-risk under Art. 6(1) and Annex I — the product-legislation route, relevant for regulated products with AI safety components.

03Engagement structure

Where the scope of an AI Act question can be defined in advance — a role-classification memo, a high-risk analysis, a readiness review — we offer it as a fixed-fee package, so that the fee is known before the work begins. The current package structure is set out on the fees page; it includes a DSA ⇄ AI Act switch that shows the corresponding packages for each regime. Matters that cannot be scoped in advance are billed transparently by time.

04Related reading

For a doctrinal analysis of how the AI Act's risk-based architecture copes with autonomous, tool-using systems, see our article Agentic AI Systems under the EU AI Act — A Risk-Based Regime Meets Its First Stress Test.

05Authorised representative under Art. 22 / Art. 54 AI Act

Separate function — not part of the law firm's mandate

Providers established outside the EU must appoint an authorised representative in the Union before placing a general-purpose AI model on the EU market; that duty follows from Art. 54 AI Act and has applied since 2 August 2025. For high-risk AI systems the parallel duty in Art. 22 AI Act was deferred by Regulation (EU) 2026/1744 and applies from 2 December 2027 (Annex III) and 2 August 2028 (Annex I). In both cases this is an operational compliance function, distinct from legal advice.

Named representative function: AI Act authorised representative under Art. 54 — a separate service of Regingada UG (haftungsbeschränkt), no legal advice. The law firm advises on the legal questions surrounding Arts. 22 and 54; the representative function itself is contracted separately with Regingada UG.

Discuss your AI Act question

Rechtsanwalt Theo Funk advises providers, deployers, importers, and distributors on the AI Act — in German and English. Describe your system and your role in the value chain; we will identify the legal questions that should be addressed first.

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