[Webinar] Maintaining product compliance – The most common mistakes and how to avoid them

A review of the key changes to EN 300 328 V2.2.2

On the 6th February 2020, the ETSI EN 2.4GHz Wideband transmission systems standard – EN 300 328 V2.2.2 – has been listed as a harmonised standard for radio equipment in support of Council Directive 2014/53/EU, also known as the Radio Equipment Directive (RED).

Global Market Access Seminar from Eurofins E&E UK and Eurofins E&E North America

Join us on the 4th & 6th December 2019 for our free seminars and learn how Eurofins E&E can help you deliver compliant products to global markets.

Why use your accredited lab for your pre-compliance testing?

Pre-compliance testing can be a critical part of the process of designing, testing and certifying a product and there are significant advantages in using the same laboratory for both your pre-compliance and full compliance testing.

[Webinar] Deal or No Deal – Your EMC BREXIT Survival Guide

With the 29th March approaching fast, now’s the time to find out how the current state of BREXIT could impact upon you and your business.

Join us for our “Deal or No Deal – Your EMC BREXIT Survival Guide” webinar and make sure you’re up to date.

UK and USA agree to continue Mutual Recognition Agreement

The UK and USA sign an agreement to continue existing arrangements which help facilitate goods trade between the two nations.

US Energy Star Certification Services Update

As of December 28th, 2018, the U.S. EPA has been closed due to a lapse in appropriations. For the duration of the U.S. government shutdown, the ENERGY STAR website and all ENERGY STAR tools, resources and data services will not be available. This includes the Qualified Products List.

EN 62368-1:2014 Certification with Eurofins York

Eurofins York is now able to offer UKAS-accredited testing of equipment to EN 62368-1:2014 at its Grangemouth laboratory.

Medical Devices – Are you ready for the 4th Edition of EN 60601-1-2?

As from the 30^th December 2018, the ^3rd edition of the collateral standard for Medical Electrical (ME) Equipment, IEC / EN 60601-1-2, will be repealed and compliance to 4^th Edition of IEC/EN 60601-1-2 will be mandatory for all medical electrical products put on the market thereafter.

Eurofins York extends its CB Scheme Accreditation to IEC 61010-2-101:2015

Eurofins York is pleased to announce that its accreditation under the CB Scheme now includes IEC 61010-2-101:2015 for In Vitro Diagnostic equipment.