Product categories that require CE Marking

The question whether the product should bear the CE marking is always in the top-3 queries of economic operators. For a quick check, please have a look at the following product categories that

What is a CE marking?

A CE marking is an important indication of the conformity of a product with the relevant European product legislation. CE stands for Conformité Européenne, feely translated, meaning: in accordance

What is a EU Declaration of Conformity?

A CE Declaration of Conformity (also called a CE Certificate) is the document certifying that the product complies with applicable law.

CE marking on industrial, commercial and residential garage doors

Five frequently asked questions about EN 1090

There are many questions about the EN 1090 standard. We answer the most frequently asked questions about this standard. Find out if your question is also listed.

New Low Voltage Directive Guidelines

New Low Voltage Directive Guidelines were published in the beginning of November. The Guidelines is a manual that explain the details of new LVD.

Eco-design for Non-directional Lamps and LED lamps

As of February 27, 2016 the Regulation (EU) 2015/1428 will formally come into force. The Regulation amends Regulation (EU) 244/2009 eco-design requirements for non-directional household lamps.

New EMC Directive 2014/30/EU

After 2014 April 2016, the CE Marking conformity assessments processes should be afdapted to the new EMC Directive 2014/30/EU. Even though the main changes are quite limited, they should be known and

Introduction to the New Machinery Regulation

The Machinery Directive is one of the most vital European product legislative Directives. The current Machinery Directive dates back to 2006. After 15 years, it became high time for a modernization, f

The major changes of the Machinery Regulations

On the 21st of April the proposal text for the new Regulation on Machinery was presented by the European Commission. The main legal changes of the proposal are summarized in this article.

EUDAMED - European Database on Medical Devices

Are you a manufacturer, authorised representative or importer of a medical device? If so, you will soon (most likely in May 2022) need to register information about yourself, your company and the medi

MDR & Implementing Regulation (EU) 2021/2226

Implementing Regulation (EU) 2021/2226 makes possible for manufacturers of medical devices to provide electronic instructions for use only. Read more about the conditions of EU 2021/2226.