EUDR Due Diligence Statements: An Essential Guide

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EUDR Due Diligence Statement

The Deforestation Regulation (EUDR) contains due diligence requirements to ensure products contributing to deforestation are not imported, sold within the EU or exported. The regulation mandates the submission of a due diligence statement, which is a document used to indicate that companies have complied with the applicable EUDR requirements.

This guide covers frequently asked questions about EUDR due diligence statements, including which types of operators are required to submit one and which are exempt.
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EU Conformity Assessment Procedures: A Complete Guide

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EU Conformity Assessment Procedures

A conformity assessment procedure provides a pathway to compliance for certain EU regulations or directives that require CE marking. In practice, conformity assessment procedures set a list of tasks that must be completed to demonstrate compliance. This generally involves compliance with standards, documentation, labelling, and testing.

In this guide, we explain how you can determine which conformity assessment procedure to follow for your products, and the steps you must take to successfully complete the procedure.
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Wood & Bamboo Product Regulations in the United States: A Complete Guide

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Products made of wood sold in the United States are subject to various regulations, standards, and other compliance requirements — which set requirements concerning documentation, chemicals, labeling, and testing.

In this guide, we take a closer look at the Lacey Act, 7 CFR Part 319 Subpart I, and other regulations relevant to companies manufacturing or importing wood and bamboo products to the United States.

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Notified Bodies in the European Union: An Overview

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Notified bodies are organisations designated by EU member countries that perform conformity assessments on products before they are sold.

The role of a notified body is to assess whether a product is technically safe and compliant. In a way, the notified body acts as a gatekeeper to the EU market for more ‘high-risk’ and ‘sensitive’ products that cannot be ‘self-assessed’.

That said, notified bodies are not government organisations. Instead, companies like Intertek and TÜV Rheinland are appointed to act as notified bodies for certain product categories.

In this guide, we explain what manufacturers and importers must know about notified bodies and how they operate.
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How to Use Test Reports from Your Supplier: A Complete Guide

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How to Use Test Reports from Your Supplier

Using existing supplier test reports can help you reduce or even eliminate the need for third-party testing when buying ODM products, materials, and components. That said, such test reports can only be used under certain circumstances. Misused, relying on supplier test reports can result in fines and recalls.

This guide provides crucial insights from more than a decade of vetting test reports from hundreds of Asian and European suppliers. We have also implemented strategies for customers that are based on partial reliance on material and component test reports.
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European Union Authorised Representatives: A Complete Guide

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Request a free EU Authorised Representative Quotation Here

Article 4 of the Market Surveillance Regulation (EU) 2019/1020 states that products can only be sold in the European Union if there is an economic operator established there. This can, for example, be an EU manufacturer or importer.

However, non-EU companies cannot function as economic operators, and therefore need an authorised representative (EU AR) that is established in the EU.

In this guide, we explain how this works in practice and what the consequences can be if you don’t have an authorised representative.

Related Articles

1. Authorised Representatives under the General Product Safety Regulation

2. List of European Authorised Representative Companies 2025

3. Responsible Persons under the General Product Safety Regulation

Note 1: This guide does not cover authorised representative requirements concerning medical devices. We have a separate article on this topic here.

Note 2: This article was updated to reflect the fact that the GPSR now extends the EU Authorised Representative requirements to other consumer products. When this guide was initially published, this was only the case for products that required CE marking.

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Packaging and Packaging Waste Regulation (PPWR): An Overview

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Packaging and Packaging Waste Regulation

The Packaging and Packaging Waste Regulation (EU) 2025/40 establishes requirements for packaging and packaging waste sold in the European Union.

This guide explains what manufacturers and importers need to know about the scope and the requirements of the regulation. This includes, substance restrictions, EPR, labelling, documentation, and more. You will also find a comparison with the requirements of the old Packaging and Packaging Waste Directive.
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Food Contact Materials Regulations in the European Union: An Overview

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Food contact materials and articles imported or manufactured in the European Union are subject to various regulations. These regulations, wihch are often collectively referred to as Food Contact Materials (FCM) regulations, cover substance restrictions, documntation, labelling, testing and other requirements.

In this guide, we list many of the key EU FCM regulations and explain when these are relevant, and break down many of their respective requirements.
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Electronics Labelling Requirements in the United Kingdom

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Electronics Labelling Requirements in the United Kingdom

Electronic products manufactured or imported for sale in the United Kingdom are subject to various labelling requirements. This includes the UKCA mark, and other compliance marks which are inherented from the time the UK was a member of the European Union.

This guide provides an overview of various labelling requirements applicable to electronic and electrical products in the UK.

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