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Archives: Resource

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....
Article 27 EU GDPR Representative

GDPR

Compliance News & Updates

Why Regulators in the EU and UK Are Increasing Checks on Article 27 EU GDPR Representative Compliance

EU and UK data protection authorities are taking a closer look at whether overseas companies have the right Article 27 EU GDPR representative in...
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...
Regulatory Compliance Software

AR, GDPR

Compliance News & Updates

The Role of Regulatory Compliance Software in Meeting UK and EU Legal Requirements

Managing regulatory obligations across the UK and EU has become more demanding for medical device companies and other regulated businesses....
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