As from the 30th 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2018, the 3rd edition of the collateral standard for Medical Electrical (ME) Equipment, IEC / EN 60601-1-2, will be repealed and compliance to 4th Edition of IEC/EN 60601-1-2 will be mandatory for all medical electrical products put on the market thereafter.
Continue reading...Meet the Eurofins team at EDS 2018 and discover the simple route to regulatory compliance.
Continue reading...Eurofins York is pleased to introduce a new Fundamentals of EMC training course that is aimed at those working in Military environments.
Continue reading...If you operate, control, or work in an environment which uses high currents or radio frequency equipment then you need to be aware of the EMF requirements in the workplace.
Continue reading...The new sections of EN 50121 which target apparatus (including rolling stock) are now listed in the Official Journal of the European Union.
Continue reading...As part of the on-going growth and development of the capabilities offered by Eurofins York, our Consultancy & Research department has been renamed to Expert Services.
Continue reading...Whether it be EMC Essentials, the Radio Equipment Directive Explained or a more advanced and in-depth course covering the Fundamentals of EMC in Railways, our extensive range of training courses always provide you with the opportunity to learn from our team of industry-recognised experts, gaining practical knowledge and guidance that you can apply to your own situation.
Continue reading...Meet the railway EMC experts at Innotrans 2018 – Stand 206R / Hall 2.2
Continue reading...June 19, 2018 – Eurofins Digital Testing, a global leader in end-to-end quality assurance and testing services, today announced that it has acquired Insite Security, a leader in information security services, to reinforce its portfolio of cybersecurity services offered to companies around the globe. Financial terms of the deal were not disclosed.
Continue reading...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.
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