Control for the European operator

The supplier completes the data. The importer governs evidence and the DPP.

NexusDPP assigns suppliers the fields within their competence while keeping checks, corrections, approval, publication and registration under the EU importer’s control.

Non-EU suppliersCountersignaturePublication gateEU Registry
The EU Registry is live

DPP registration can be integrated into the importer workflow.

Since 20 July 2026, the EU Registry has provided a secure user interface and API. Where product legislation requires a DPP, NexusDPP can coordinate data approval, identifiers, metadata submission, error handling and electronic proof of registration. A live Registry does not, however, make a DPP mandatory for every product; scope depends on the applicable legislation.

How the Registry works
DPP caseImported product · N24
EU importer
Required fields48
Received42
To correct3
  1. Request sent to manufacturerAccess limited to relevant data
    Completed
  2. Documents and data receivedSource, version and date recorded
    Completed
  3. 3
    Importer reviewCorrections and additions in progress
    In review
  4. 4
    Approval and countersignatureGate before publication and registration
    Waiting
The importer’s challenge

Collecting information properly means being able to demonstrate compliance with confidence.

Technical sheets, composition, origin, certificates and conformity evidence are collected in one process, with coordinated versions and systematic checks.

  • Repeated requests and long lead times with distant suppliers.
  • Missing fields discovered only at the end of the process.
  • Difficulty linking each document to the correct model, batch or component.
  • Regulatory pressure and commercial risk concentrated on the EU operator.
Legal responsibility

The importer plays a direct role in product compliance.

For consumer products, Article 11 of Regulation (EU) 2023/988 sets out general obligations for importers. These are complemented by Regulation (EU) 2019/1020 on market surveillance and by the rules applying to the specific product category.

Checks before placing on the market

Verify that the manufacturer has fulfilled the applicable obligations, that the product is identifiable and that the required documentation, instructions, warnings and safety information are available.

Blocking non-compliant products

Where there are reasons to believe that a product is dangerous or non-compliant, the importer must suspend its placing on the market and initiate the required corrective measures.

Importer identification

The importer’s name or trade name, postal address and any electronic contact details must appear on the product, packaging or accompanying documents, in accordance with the applicable rules.

Storage and transport

Storage and transport conditions under the importer’s responsibility must preserve product safety, integrity and compliance.

Traceability and authorities

The importer must retain the necessary information, manage reports and complaints, cooperate with authorities and provide data and documents useful for market surveillance.

Products under the importer’s own brand

An operator marketing a product under its own name or trademark, or substantially modifying it, may assume the manufacturer’s obligations under Article 13 of Regulation (EU) 2023/988 and the applicable sector legislation.

Penalties and risks

Across Europe, infringements can have a significant economic and operational impact.

Regulation (EU) 2023/988 requires Member States to apply effective, proportionate and dissuasive penalties. Amounts and measures vary according to the country, product category and seriousness of the infringement.

Administrative and financial penalties

Penalties may apply to dangerous or non-compliant products, inadequate documentation, missing information, failure to meet traceability obligations or failure to cooperate with authorities.

Sales restrictions or suspension

Authorities may require corrective action, suspend marketing, prohibit making the product available, or order withdrawal or recall.

Operational and reputational costs

Relabelling, new testing, replacements, reverse logistics, contractual disputes and loss of trust can have a greater impact than the penalty itself.

Operational risks

Non-compliance can stop the product.

Beyond financial consequences, an authority’s measure can interrupt distribution and require rapid action on products already placed on the European market.

  • Suspension of sales and distribution delays.
  • Costs for verification, rework, relabelling, withdrawal or recall.
  • Lost orders, contractual disputes and reputational damage.
  • Greater exposure of the EU operator to authorities, distributors and customers.
NexusDPP method

Request → Collect → Validate → Approve → Publish.

The workflow distributes the work while maintaining control, accountability and visibility over the process. Each party sees only what it must complete, approve or verify.

Secure invitation

The supplier receives dedicated access and a precise request for a product or model.

Guided completion

Fields, units of measure, required attachments, deadlines and instructions in the project language.

Completeness checks

The platform flags omissions, invalid formats, expired documents and inconsistencies.

EU approval

The importer reviews, requests corrections and authorises progression to the next status.

QR or NFC

Unique identifier and data carrier associated with the product, batch or individual unit.

Updates over time

Versions, document changes, recalls, support and end-of-life events remain connected.

Optional module

Trade Compliance for international supply chains and shipments

Document counterparty screening, final destination, end users, clauses and logistics documents in one audit trail.

Explore the module