IN BRIEF

Supplier due diligence for AI should ask for the information needed to assess the system and the supplier's role, test supplier claims against evidence, record gaps as open items, and set contract terms for information flow, updates, incidents and change notification. A supplier's marketing claim, certificate, or assurance is not a substitute for the evidence the deployer or provider needs for its own assessment, and due diligence must continue after procurement, through monitoring and reassessment.

01 / IMPLEMENTATION AND GOVERNANCE

What questions should be asked before procurement?

Before procurement, the buyer should ask for the system's intended purpose and use limits, the provider and deployer roles, the classification analysis, the testing and performance evidence, the data governance and bias examination, the human oversight design, the transparency and marking position, the logging and monitoring capability, the incident and update processes, and the documentation that will be supplied. Each question should be tied to a decision the buyer must make: whether the system fits the intended use, whether it is high-risk, what oversight and monitoring it needs, and what evidence the buyer must keep. Questions should be asked in writing, with a named supplier contact, and the answers should be recorded with the date and version, so that a later dispute about what was said can be resolved from the record. A procurement process that asks only about price, features, and delivery date has not carried out AI due diligence.

02 / IMPLEMENTATION AND GOVERNANCE

How should supplier evidence be tested?

Supplier evidence should be tested, not taken at face value. The buyer should check that the documentation matches the system version to be supplied, that test results reflect the buyer's deployment context, that limitations are stated, and that conformity, registration, and declaration records exist where the Act requires them. The buyer should sample the evidence, ask follow-up questions where it is incomplete, and record the gaps as open items with owners and dates. Where a supplier cannot provide evidence for a material question, the buyer should assess whether the system can be deployed without that evidence, whether additional testing or controls are needed, or whether procurement should be paused. A supplier assurance that evidence will be provided later, without a date and a contractual commitment, should be treated as an open gap, not as evidence.

For the broader regulatory framework, see AI governance planning checklist.

03 / IMPLEMENTATION AND GOVERNANCE

What contract terms matter for AI Act work?

Contract terms should cover the information to be supplied and updated, including downstream information for models, instructions for use for systems, and change notification, the timetable for updates and incident reporting, the right to audit or to receive evidence, the allocation of roles and responsibilities, the handling of data protection and confidentiality, and the consequences of a supplier failure to provide information or to take corrective action. Terms should be specific to the system and version, with named contacts and response times, rather than generic statements about cooperation. The contract should also address what happens if the supplier changes the system, withdraws it, or ceases to support it, including data, log, and documentation handover. A contract that labels roles without addressing information flow and change control does not support the buyer's AI Act work, even if it is commercially complete.

04 / IMPLEMENTATION AND GOVERNANCE

How should suppliers be monitored after procurement?

Monitoring should include regular checks that the supplier's information remains current, that updates and incidents are notified as agreed, that performance and oversight remain as assessed, and that any change to the system, its data, or its purpose is communicated. The buyer should set a review cadence, assign an owner, and record each review, with findings and follow-up actions. Monitoring should also include feedback from operational staff, complaints, and log patterns, fed back to the supplier through the agreed channel. A supplier relationship that ends at procurement, with no monitoring, will miss changes that affect the buyer's assessment, and the buyer will discover the change only when an incident or an authority question reveals it. Monitoring records should be linked to the inventory and the change register for the system.

05 / IMPLEMENTATION AND GOVERNANCE

What are the limits of supplier assurances?

Supplier assurances have limits. A supplier cannot assess the buyer's deployment context, affected people, or oversight design, and cannot carry out the buyer's deployer duties, including a FRIA where one is required. A certificate or a conformity record for the supplier's system does not prove that the system is suitable for the buyer's specific use, and a general-purpose model pack does not settle a downstream system assessment. The buyer must carry out its own assessment, using supplier evidence as an input, and must record its own reasoning and decisions. Where a supplier's assurance conflicts with the buyer's own testing or operational experience, the conflict should be recorded, raised with the supplier, and resolved with evidence, rather than resolved by preferring the assurance because it is more convenient.

Continue with AI governance operating model.

06 / IMPLEMENTATION AND GOVERNANCE

What does this guide not decide?

This guide does not decide whether a particular supplier has met its duties, whether a system is suitable for a specific deployment, or whether a contract term is sufficient. It does not assess a supplier, a product, or a procurement decision. Those questions depend on the supplier evidence, the system, the deployment context, the contract, and the consolidated legal text. A buyer should carry out due diligence in writing, test the evidence, record gaps as open items, and confirm the position with a competent authority or legal adviser where the supplier position is material to a high-risk deployment.

FAQ / PRACTICAL QUESTIONS

Frequently asked questions

Is a supplier's CE marking enough for a deployer?

No, on its own. CE marking and the declaration evidence the provider's conformity assessment for the system, but the deployer must still assess its own deployment, follow instructions, assign oversight, monitor operation, and carry out a FRIA where required. Supplier evidence is an input to the deployer's assessment, not a substitute for it.

What if a supplier will not provide evidence?

Record the gap as an open item, assess whether deployment can proceed without the evidence, whether additional testing or controls are needed, or whether procurement should pause. Do not close the gap by assumption, and raise it through the contract route with a date for the evidence to be supplied.

How often should suppliers be reviewed?

Set a review cadence proportionate to risk and volume, with triggers for change, incident, or new guidance. Record each review, the findings, and the follow-up, and link the review to the inventory and change register for the systems the supplier provides.

RELATED / CLUSTER PATHWAYS

Continue through this AI Act cluster

Verify the source

This article is an informational overview, not a legal determination. Check the current legal text and official implementation guidance for your system and role.

Consolidated Regulation (EU) 2024/1689 ↗Commission AI Act Service Desk timeline ↗European Commission AI Act overview ↗