european union

Many manufacturers believe that third-party testing is required to meet the requirements of the EU’s EMC Directive. But there are other, legally acceptable paths to demonstrate compliance with the EMC Directive that do not require the use of a third party.

The Commission of the European Union (EU) has updated the list of harmonized standards used in the process of accrediting laboratories involved in the development or assessment of medical devices.

The EU Commission has published detailed regulations for the cybersecurity certification of certain products, taking the next step in implementing an EU-wide cybersecurity certification scheme.

The U.S. and the European Union have signed an agreement to work collaboratively to strengthen the cybersecurity of IoT-capable hardware and software products used by consumers.

The Commission of the European Union (EU) has proposed providing manufacturers of certain medical...

This article reflects on the recent drafting of a European circular product standard, the publication of EN4555X material efficiency standards, and some specific international and national standards. This standardization activity is spearheading thinking on resource efficiency, and the requirements of these standards could soon find their way into future EU ecodesign laws.

The Commission of the European Union (EU) has recently adopted three separate legislative proposals...

The goal line is in sight for legislators in the European Union (EU) in...

A consortium of medical technology companies in the European Union (EU) has published a...

The Commission of the European Union (EU) has extended the effective date of its...