Quick summary: Learn how EUDR DDS consolidation and Article 8a grouping work, what data to validate, and how to manage declarations with confidence.
EUDR DDS consolidation helps businesses streamline declaration management, reduce administrative complexity, and improve supply chain efficiency while maintaining the traceability, due diligence evidence, and regulatory controls required under the EU Deforestation Regulation (EUDR). For businesses sourcing EUDR-regulated products such as coffee, cocoa, rubber, soy, palm oil and wood, managing Due Diligence Statements (DDS) can become complex as supplier, plot and shipment volumes grow. EUDR DDS consolidation can mean organising data from multiple sources for a correctly scoped declaration, or grouping declarations already submitted under Article 8a of the Information System rules.
These are different activities. A larger declaration is not automatically compliant, and grouping does not remove due diligence obligations.
Operationally, consolidation can mean bringing supplier, production-area, commodity, quantity and evidence data into one controlled workflow. Whether multiple sources can be covered by a single DDS depends on the transaction and applicable requirements. The declaration must accurately represent the products placed on the EU market or exported, with due diligence completed for all sources covered.
Article 8a is a separate capability: users can submit a new DDS or simplified declaration referencing previously submitted declarations by their reference numbers or identifiers. The originals receive a grouped status, and the grouped declaration represents them for EUDR compliance purposes. This manages references; it does not fix incomplete data or bypass due diligence.
Commission Implementing Regulation (EU) 2026/1565, adopted on 13 July 2026, introduced Article 8a to the EUDR Information System rules. The change addresses technical constraints associated with declaration files and aims to reduce disruption to customs procedures.
Under Article 8a, an Information System user can group previously submitted DDS or simplified declarations by creating a new declaration that references them. The grouping is available for declarations submitted by the same Information System user, or, where applicable, for the same operator or micro or small primary operator by an authorised representative. Once grouped, the original declarations are marked accordingly in the system, and the grouped declaration’s reference number or identifier can be communicated in place of the individual references for the purposes specified in the regulation.
The grouped declaration must still be complete in its own right. Official Information System API documentation explains that the group head must state the relevant products, quantities, HS codes and other required data that reflect what is actually being placed on the market or exported. The system does not automatically reconcile all product and quantity information from the referenced declarations, so operators remain responsible for the accuracy of the group head.
Explore how to streamline compliance processes, manage due diligence requirements, and prepare your supply chain for EUDR implementation.
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Consider a coffee exporter working with several cooperatives and hundreds of farm plots. The exporter needs to connect supplier records and plot-level geolocation to the coffee lots, processing batches and export consignment. A structured data workflow can bring those records together for a correctly scoped DDS, provided all relevant information and due diligence requirements are satisfied.
Now consider a business that has already submitted several declarations and needs a simpler way to communicate their references. Article 8a grouping may help by creating a grouped declaration that references those prior submissions. This can be useful for high-volume operations, but the grouped declaration still needs accurate product and quantity details, and the referenced records must be tracked carefully.
Ask: “Does this declaration accurately represent the transaction, and can we retrieve evidence for every product and source it covers?”

Spreadsheets and email become difficult to manage across hundreds of suppliers, thousands of plots and multiple shipments. An EUDR platform can connect supplier onboarding, geolocation validation, risk assessment, evidence, batch traceability and declaration references.
Look for pre-submission validation, quantity reconciliation, source-to-product links, status tracking and quick evidence retrieval. Procurement, ERP and logistics integrations can reduce duplicate entry, while approval workflows help catch errors.
TraceX connects supplier and farm data, geolocation, traceability, risk and evidence with products, batches and shipments. This can reduce manual reconciliation and improve visibility, while regulatory responsibility remains with the operator.
EUDR DDS consolidation works best when efficiency is built on trustworthy data. Article 8a provides a formal way to group eligible submitted declarations, while a well-designed workflow connects each DDS to the products and sources it represents.
EUDR DDS Consolidation means organising data from multiple suppliers or plots into a correctly scoped DDS, or more specifically to grouping previously submitted declarations under Article 8a. These are different activities and should not be confused.
Yes. Article 8a allows an Information System user to submit a new DDS or simplified declaration that references eligible previously submitted declarations. The referenced declarations receive a grouped status, and the grouped declaration represents them for EUDR compliance purposes.
No, DDS Grouping does not remove the need for due diligence, operators remain responsible for due diligence and for the accuracy of the relevant product, quantity and supporting information. Grouping does not resolve missing geolocation, weak evidence or an incomplete risk assessment.
No. The European Commission’s Information System API documentation states that the group head must be a complete declaration in its own right and that operators are responsible for entering correct product and quantity information.
Companies can prepare for DDS Consolidation by creating a reliable register connecting suppliers, production areas, products, quantities, batches, shipments and DDS references. Validate data before filing, maintain evidence, define approval controls and test the process with real transaction scenarios.