Tag: compliance eu

Unsafe and non-compliant products can be subject to recalls. This essentially means that you as a seller must arrange the return, replacement, and possible refund of the affected product. Product recalls are incredibly expensive and can spell disaster for smaller businesses.

Further, products can be subject to a recall for a variety of reasons, including chemical content, design safety flaws, incorrect labeling, and documentation.

In this guide, we help importers and manufacturers better understand how the recall process works in the EU. We also cover common safety hazards that can lead to a recall, the EU RAPEX system, and Amazon’s policy on product recalls. Continue reading European Union Product Recall Guide For Importers and Manufacturers

User instructions are generally speaking documents explaining how to install, properly use, and dispose of products. User instructions can also include battery replacement instructions, warning texts, and more.

While consumers often take user instructions for granted, many importers and manufacturers overlook the fact that user instructions are mandatory for a wide range of products in the European Union. Hence, failing to create a sufficient user instruction document can result in fines or a product recall.

Keep reading, and learn the basics that importers, manufacturers, and Amazon sellers must know about creating user instructions for electronics, toys, and many other consumer products. Continue reading Product User Instructions Requirements in the European Union: An Overview

Planning or import or manufacture supplements in the European Union? In this guide, we cover the basics of substance restrictions, labeling, notification, documentation, and lab testing requirements for a range of supplements products in the EU.

Supplements are considered as food products in the EU and are mainly regulated by Directive 2002/46/EC – which we cover in more detail in this guide. That said, other regulations may apply if the supplements contain colorants or sweeteners. Continue reading Supplement Regulations in the European Union: An Overview

The role of a Notified Body is to assess if a product is technically safe and compliant, correctly documented, and (in some cases) manufactured under the right conditions. In a way, the Notified Body act as a gatekeeper to the EU market – for more ‘high-risk’ and ‘sensitive’ products that cannot be ‘self-certified’.

That said, Notified Bodies are not government organizations. Instead, companies like Intertek and TUV are appointed to act as Notified Bodies for certain product categories.

In this guide, we explain what importers, exporters, and manufacturers must know about Notified Bodies and how they operate. Continue reading Notified Bodies in the European Union: A Complete Guide

Product traceability requirements exist to ensure that products can be traced to a certain importer or manufacturer, production facility, SKU, and even production run. The latter is particularly important as it enables market surveillance authorities (and sellers) to identify and trace unsafe and non-compliant products – and thereby limiting product recalls to faulty batches.

Product traceability labeling is mandatory for a wide range of products, such as electronics, kitchen products, toys, and much more. Still, product traceability is often overlooked by importers and manufacturers.

Keep reading, and learn what importers and manufacturers must learn about different types of product traceability requirements in the European Union. Continue reading Product Traceability Requirements in the European Union: An Overview