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ENEC+ Mark

We are proud to announce that SIQ Ljubljana has successfully passed the assessment by the Slovenian Accreditation to be a step closer to membership in the ENEC+ Scheme.  This year we obtained new equipment for measuring photome...

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Efficiency and No-Load Power Consumption

The latest eco-design requirements for external power supplies are laid down in Commission Regulation (EU) 2019/1782 regarding the efficiency and no-load power consumption that repeals Commission Regulation EU 278/2009. The lat...

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New RoHS Requirements for Electrical and Electronic Equipment for Saudi Arabia

A new Technical Regulation on the restriction of hazardous substances in electrical and electronic equipment (RoHS) has recently been introduced by Saudi Standards, Metrology and Quality Organization (SASO). This regulation applies to the ...

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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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The safety of medical devices

At SIQ, we started testing the safety of medical devices 25 years ago, mainly led by the desire to help Slovenian manufacturers place their innovative medical products on the Slovenian and international market. In 2005, a new c...

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