EU AI ActChecklist

EU AI Act (Regulation (EU) 2024/1689) Compliance checklist

A useful checklist is a list of outputs, owners, and review points.

This checklist is structured so teams can move from scoping to evidence instead of collecting generic policy language.

Author
Sorena AI
Published
Mar 4, 2026
Updated
Mar 4, 2026
Sections
6

Structured answer sets in this page tree.

Primary sources
5

Cited legal and guidance references.

Publication metadata
Sorena AI
Published Mar 4, 2026
Updated Mar 4, 2026
Overview

The AI Act does not reward broad statements about responsible AI. It rewards accurate classification, complete evidence, and operating controls that still work after launch. Use this checklist by system and by model, then track gaps in the same delivery tooling you use for security and product work.

Section 1

Portfolio and scoping foundation

Before you touch technical controls, make sure the system is registered, scoped, and assigned to the right role owners. Every later obligation depends on this layer being correct.

This is also the point where many teams catch shadow AI use, unapproved model APIs, and downstream resale arrangements that were never reflected in the compliance record.

  • AI system register complete with intended purpose, owner, deployment context, and model dependencies.
  • Role matrix complete for provider, deployer, importer, distributor, and authorised representative where relevant.
  • Exclusions and open source position documented with article basis.
  • Reassessment triggers documented for model changes, new uses, and substantial modification.
Section 2

Article 5 and AI literacy controls

The earliest live obligations are not optional extras. Prohibited practice screening and AI literacy should be operating controls, not one time training slides.

The screening outcome should be attached to release approvals and high impact design reviews.

  • Article 5 screening completed before launch and on material changes.
  • Escalation path exists for manipulative techniques, vulnerability exploitation, prohibited biometrics, and social scoring concerns.
  • Article 4 AI literacy training is assigned to product, operations, support, and oversight roles.
  • Training completion and role specific guidance are retained as evidence.
Section 3

High risk system controls

If a system is high risk, the evidence standard changes completely. You need a lifecycle assurance set built around Articles 9 to 15 and the provider and deployer duties that sit around them.

Do not stop at a risk register. High risk evidence has to cover technical documentation, human oversight, logging, post market monitoring, and authority facing records.

  • Article 9 risk management system documented and maintained across the lifecycle.
  • Article 10 data governance controls and data quality evidence complete.
  • Article 11 Annex IV technical documentation plan complete and version linked to releases.
  • Articles 12 to 15 logging, instructions, human oversight, accuracy, robustness, and cybersecurity controls evidenced.
  • FRIA, affected person notices, EU database registration, conformity route, and CE marking checked where applicable.
Section 4

Transparency and user disclosure controls

Article 50 work belongs in product delivery, content operations, accessibility review, and analytics. If users interact with AI or receive synthetic content, the disclosure logic must be built into the interface and into the release process.

Where machine readable marking is required, product teams should treat it as a technical feature with QA evidence, not as marketing copy.

  • Direct interaction notices mapped to all relevant product surfaces.
  • Synthetic image, audio, video, and text marking triggers documented.
  • Deepfake and public interest publication disclosures reviewed with editorial owners.
  • Display evidence, screenshots, and privacy minimised logging retained.
Section 5

GPAI provider and supplier controls

Chapter V applies at model level. If you provide a GPAI model, you need technical documentation, downstream information, a copyright policy, and a public summary of training content. If you rely on a third party GPAI provider, you need contract and evidence demands that let your system level compliance continue to work.

Systemic risk scenarios need a higher state of readiness because notification, safety and security, and serious incident reporting duties tighten.

  • Article 53 technical documentation and downstream documentation workflow in place.
  • Copyright policy maintained and linked to data sourcing governance.
  • Public summary of training content prepared using the AI Office template where required.
  • Article 52 systemic risk notification path and Article 55 serious incident reporting process defined.
  • Supplier clauses require version notices, technical documentation extracts, and incident cooperation.
Section 6

Authority ready evidence pack

Your final test is simple: if a buyer, regulator, or partner asks for evidence tomorrow, can you produce a coherent file without rebuilding the story from scratch?

The evidence pack should be kept current and tied to actual versions, not abstract program material.

  • Decision records for applicability, high risk status, transparency, and GPAI duties.
  • Release linked technical documentation, instructions, and test records.
  • Incident, complaint, and corrective action workflow records.
  • Named owners, last review dates, and next review triggers for every major artifact.
Recommended next step

Turn EU AI Act (Regulation (EU) 2024/1689) Compliance checklist into an operational assessment

Assessment Autopilot can take EU AI Act (Regulation (EU) 2024/1689) Compliance checklist from turning this checklist into an operational workflow to a reusable workflow inside Sorena. Teams working on EU AI Act (Regulation (EU) 2024/1689) can keep owners, evidence, and next steps aligned without copying this guide into separate documents.

Primary sources

References and citations

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