EUDR operational reference

EUDR due diligence: the three steps and DDS requirements

Due diligence under the EU Deforestation Regulation (EUDR) has three steps: collect the required information, assess the risk, and mitigate any risk that is more than negligible. You must complete the applicable process before placing a relevant product on the EU market or exporting it.

The Due Diligence Statement (DDS) records the result. It does not replace the evidence, checks, and decisions behind it. Those belong in your due diligence system and must be available if a competent authority asks for them. A controlled regulatory operations model keeps that evidence tied to the submitted record.

The decision rule

Missing required information means the product cannot proceed. More than negligible risk means the product cannot proceed. Filing a DDS does not make weak evidence compliant.

The EUDR due diligence process in three steps

These are not internal labels. They come from Article 8 of the EU Deforestation Regulation, which defines due diligence as the three actions below. The links open the relevant provisions in the current consolidated legal text.

01

Collect the required information

Article 9: information requirements

Identify the product, quantity, and country of production. Connect every relevant commodity to its production plots or cattle establishments, production dates, suppliers, and customers. Hold verifiable evidence that it is deforestation-free and legally produced.

02

Test the information for reliability and completeness. Consider country risk, forest and deforestation conditions, Indigenous Peoples' rights, legality, supply-chain complexity, mixing, and circumvention. Record how you reached the result.

03

Mitigate any risk above negligible

Article 11: risk mitigation

Request more evidence, commission surveys or audits, improve controls, or support suppliers. Do not place the product on the market or export it until the remaining risk is no more than negligible.

Step 1: information required for EUDR due diligence

Article 9 sets the minimum information. A supplier certificate or purchase order is not enough. The records must connect the exact product to its production origin and support both the deforestation-free and legality findings.

Core Article 9 information that an operator must collect before assessing risk.
Information groupWhat the record needs to establish
ProductDescription, trade name and type; relevant commodities or products; wood species where applicable.
QuantityNet mass and, where required, the applicable supplementary unit; otherwise mass, volume, or number of items.
Production originCountry of production and, where relevant, the part of the country.
Production placesGeolocation of every relevant plot or cattle establishment, with the production date or time range.
Supply chainNames, postal addresses, and email addresses of relevant suppliers and recipients.
Deforestation-free evidenceConclusive and verifiable information showing compliance with the 31 December 2020 cut-off.
Legality evidenceConclusive and verifiable information showing compliance with relevant laws in the country of production.

Geolocation is product evidence

A supplier address is not production geolocation. The record must cover every relevant production plot or cattle establishment and the applicable production date or range. If a product combines commodities from several plots, every relevant plot must be included.

Step 2: carry out and document the risk assessment

An EUDR risk assessment is not a supplier score alone. It tests whether the Article 9 evidence supports compliance for the particular products and supply chain. The conclusion must be documented and reviewed at least annually, and whenever relevant information changes.

The assigned risk level of the country or region of production

The presence of forests, deforestation, or forest degradation

The presence, consultation, and reasoned land claims of Indigenous Peoples

Corruption, weak enforcement, falsified records, conflict, or sanctions

The reliability, validity, and connection of the evidence

Supply-chain complexity and difficulty tracing goods to production land

Mixing, circumvention, and links to unknown or non-compliant sources

Substantiated concerns and the compliance history of the supply chain

What negligible risk means under EUDR

Article 2(26) of the EUDR

Negligible risk is the documented conclusion reached after assessing the product-specific and general information, and applying mitigation where needed, when there is no cause for concern that the product is not deforestation-free or was not produced in accordance with the relevant laws of the country of production.

It is not a percentage, a fixed score, or the same as sourcing from a low-risk country. If material gaps, contradictions, unreliable evidence, or credible concerns remain unresolved, the risk is not negligible.

Required outcome

No risk or only negligible risk

Your record should show what was checked, what concerns were found, how they were resolved, and why no cause for concern remains. If it cannot, move to risk mitigation. Do not place the product on the market or export it.

Step 3: mitigate risk before the product proceeds

Risk mitigation must be adequate and proportionate to the problem found. It may mean obtaining stronger documents, checking source data, commissioning an independent survey or audit, changing controls, separating uncertain material, or helping a supplier produce reliable evidence.

Record the concern, the action taken, the new evidence, and why the remaining risk is negligible. A mitigation log that ends with “accepted by compliance” but does not explain the decision is difficult to defend.

Simplified due diligence is not no due diligence

Where all relevant products and commodities covered by the assessment were produced in countries or regions classified as low risk, Article 13 relieves the operator of the Article 10 risk assessment and the Article 11 mitigation steps — and of nothing else. The Article 9 information still has to be collected, and a normal Due Diligence Statement is still submitted under Article 4.

This is not the same as the simplified declaration. That is a separate regime under Article 4a, available only to micro and small primary operators, which file a one-time declaration and may give the postal address of their plots or establishment instead of geolocation. A standard operator sourcing from a low-risk country does not qualify for it.

If new information or a substantiated concern indicates possible non-compliance or circumvention, the operator must complete the full process. Country classification does not override contrary evidence about a product or supply chain.

What goes into an EUDR Due Diligence Statement?

A DDS is a structured declaration submitted through the EUDR Information System. Per Annex II it identifies the operator, the relevant product, the quantity, the country of production, and the geolocation of every relevant plot or cattle establishment. It also records the operator’s declaration that due diligence was carried out and found no or only negligible risk.

The production date or time range is not among the submitted fields. It is Article 9 information the operator must collect, organise, and keep for five years — so an implementation should hold it in the due diligence record and must not require or validate it as part of the submission payload.

The DDS contains

The submission fields and the operator’s compliance declaration.

The due diligence system contains

The source evidence, checks, risk reasoning, mitigation, and approval record behind the declaration.

Submit the DDS or simplified declaration before placing the product on the market or exporting it. For imports, its reference number or declaration identifier must be available before the customs declaration is lodged. One DDS may cover several batches or shipments, but not more product than the quantity it declares.

Certification can support the evidence. It cannot replace the process.

Certification and third-party verification can be useful supporting information. They may help establish production practices, chain of custody, or legality. They do not transfer the legal responsibility away from the operator.

Check what the scheme actually verifies, whether it covers the same product and production land, how current the evidence is, and whether it addresses every applicable EUDR requirement. Include it as one part of the documented assessment rather than treating the certificate as the conclusion.

Worked example: one coffee shipment

01

Connect the shipment to production

The importer records the coffee product and quantity, country and region, farms and plot coordinates, harvest period, supplier, and evidence of legal production and no deforestation after 31 December 2020.

02

Test the evidence and supply chain

The importer checks whether every farm is represented, whether the coordinates match the production records, whether mixing occurred, and whether country, legality, or deforestation indicators create more than negligible risk.

03

Resolve the gap, then file

One farm lacks a reliable production date, so the importer requests better records and holds the shipment. Once the evidence closes the risk, the decision is recorded and the DDS is submitted before the customs declaration.

Due diligence system, records, and review

5 years

Retain due diligence records and system updates.

Annual

Review the system at least once each year.

Immediate

Act when new information indicates possible non-compliance.

Non-SME operators also have public reporting and stronger internal-control requirements. The system should show who owns compliance decisions, how evidence is checked, how exceptions are escalated, and what prevents an unapproved product from proceeding.

Common questions

What does negligible risk mean under EUDR?
Under Article 2(26), negligible risk is the conclusion reached after assessing the product-specific and general information, and applying mitigation where needed, when there is no cause for concern that the product is not deforestation-free or was not produced in accordance with the relevant laws of the country of production. It is not a numeric threshold. Unresolved gaps, contradictions, unreliable evidence, or credible concerns mean the risk is not yet negligible.
What are the three steps of EUDR due diligence?
The three steps are collecting the information required by Article 9, assessing the risk of non-compliance under Article 10, and mitigating any risk that is more than negligible under Article 11. An operator must reach no or only negligible risk before placing a relevant product on the EU market or exporting it.
What must an EUDR due diligence statement contain?
Per Annex II, a DDS identifies the operator, the relevant product and commodity, the quantity, the country of production, and the geolocation of every production plot or cattle establishment. It also includes the operator's declaration that due diligence was carried out and found no or only negligible risk. The production date or time range is an Article 9 information requirement that the operator collects and retains — it is not a field in the submitted statement. The evidence and assessment behind the declaration likewise remain in the operator's due diligence system.
What is simplified due diligence under EUDR?
Two different things are often confused. Simplified due diligence under Article 13 applies when all relevant commodities and products covered by the assessment were produced in countries or regions classified as low risk: the operator is relieved only of the Article 10 risk assessment and the Article 11 mitigation steps. The Article 9 information must still be collected, and a normal DDS is still submitted under Article 4. Separately, the one-time simplified declaration under Article 4a is available only to micro and small primary operators, which may give the postal address of the plots or establishment instead of geolocation. If relevant information or a substantiated concern indicates possible non-compliance or circumvention, the full risk-assessment and risk-mitigation process must be completed.
Can certification replace EUDR due diligence?
No. Certification and third-party verification may support the evidence, but they do not replace the operator's legal responsibility. The operator must still collect the required information, assess risk, mitigate any risk that is more than negligible, and submit the applicable DDS or simplified declaration.
How long must EUDR due diligence records be retained?
Operators must retain due diligence records for five years from the date a relevant product is placed on the EU market or exported. This includes the information collected, risk assessments, mitigation decisions, procedures, and updates to the due diligence system.
Can one EUDR DDS cover multiple shipments?
Yes. One DDS can cover multiple batches or shipments when all products are covered by the due diligence and the legal requirements are met. Once the quantity covered by that DDS has been used, a new DDS is needed for additional quantities.
When must an EUDR DDS be submitted?
The applicable DDS or simplified declaration must be submitted before the relevant product is placed on the EU market or exported. For imports, the reference number or simplified-declaration identifier must be available before the customs declaration is lodged.
Do downstream operators and traders repeat upstream due diligence?
Not automatically. Under the current framework, non-SME downstream operators and traders must verify upstream due diligence when they obtain or become aware of information indicating a substantiated concern. They must not place, make available, or export the product unless that verification shows no or only negligible risk.

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Sources and currency

Editorial owner: Invaritech. Last reviewed against primary sources on 15 August 2026. EUDR has been amended and delayed more than once — confirm the current position against the official sources below before acting. This is an operational reference, not legal advice.

Governing instruments: Regulation (EU) 2023/1115, as amended by Regulation (EU) 2025/2650. Commission Implementing Regulations (EU) 2024/3084 and (EU) 2026/1565.