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Category: Industry Insights

CE Marking on Medical Devices

Medical devices

Industry Insights

CE Marking on Medical Devices What Recent EU MDR Updates Mean for UK Exporters

Exporters of medical devices face a shifting regulatory environment in the European Union and the United Kingdom....
EPREL Registration for EU Energy-Labelled Products(thumbnail)

EPREL

Regulatory Framework

How to Register Products in EPREL: Step-by-Step Guide for EU Energy Labelling

EPREL registration is required for energy-labelled products sold in the EU, but it is often misunderstood. This guide explains the process and common pitfalls....
Responsible Person Cosmetics Brexit

Cosmetics

Industry Insights

How Brexit Changed the Role of the Responsible Person Cosmetics Requirement in the UK and EU

Brexit refers to the United Kingdom leaving the European Union. While the change was political, its impact on product compliance has been very practical...
Amazon AHD Verification for E-Mobility Devices thumbnail

Electric Devices

Regulatory Framework

Amazon AHD Verification for E-Mobility Devices: Battery, Electrical & Testing Requirements (EU and UK)

E-mobility devices face heightened scrutiny on Amazon due to their batteries and electrical components. This guide explains AHD verification requirements for EU and UK...
data protection representative

AR, GDPR

Compliance News & Updates, Industry Insights

New EU and UK Enforcement Actions Spotlight the Need for a Data Protection Representative

For businesses selling physical products into the EU or UK from outside these regions, appointing a GDPR Representative under Article 27, sometimes informally referred...
IVDs vs Medical Devices Choosing the EU Route- thumbnail

Medical devices

Industry Insights

IVDs vs Medical Devices: How to Identify the Correct EU Regulatory Pathway

Misclassifying a product under the EU MDR or IVDR can lead to delays and compliance issues. This article explains how to identify the correct...
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