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Product Testing and Certification

IEC 61326-2-6: In vitro diagnostic (IVD) medical equipment – EMC requirements

We would like to inform you of the new edition of the standard that covers EMC testing of in-vitro (IVD) medical equipment – IEC 61326-2-6:2020. Newer versions of standards usually introduce minor changes to the already established and accepted te...

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Laboratory, Control, and Measurement Devices: New Edition of IEC/EN 61326-1 is Here

We would like to kindly inform you about a new edition of the standard that covers EMC testing of electrical equipment for measurement, control, and laboratory use – IEC 61326-1:2020 – and its recently issued EN version EN IEC 61326-1:2021.

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Changes and Impacts of the new EN 60601-1:2006 + A1:2013 + A2:2021(Amendment 2)

In June 2021, Amendment 2 to EN 60601-1 (also referred to as Version 3.2 of IEC 60601-1) was published on the Cenelec web page. The most significant changes are: Updated terms and definitions to align with a new ed...

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SIQ is accredited to perform testing according to the new amendment IEC 60601-1-2:2014 + A1:2020

In 2020, a new amendment A1 was published that made some changes to IEC 60601-1-2:2014. The crucial changes: Conducted disturbances (conducted emissions) shall be performed at min. and max. RATED voltage, ...

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Mandatory use of new amendment A1 of EN 61010-1 (Safety requirements for electrical equipment for measurement, control and laboratory use) from 2022

Mid of next year, amendment A1 to EN 61010-1 will become mandatory. Though issued some time ago and already widely used at SIQ, we would like to notify our partners that this amendment will be mandatory in the EU as of 30th May 2...

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