Product Testing and Certification
The ‘Blue Guide’ on the implementation of EU product rules 2022
This new version of the Guide builds on the past editions, but also reflects recent changes in the legislation and in particular the adoption of a new Regulation on Market Surveillance. Historically, the EU legislation for goods has progressed ...
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Social activities at SIQ: surfing and water skiing
On a lovely Monday morning of July 18, a group of colleagues headed to Wake Park Dooplek in Spodnji Duplek near Maribor. The Wake Park Dooplek is the first surfing and water-skiing park in Slovenia. They had a wonderful time, which can also be ...
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SIQ issues the 10000 CB certificate
We are proud to announce that in September SIQ issued a certificate with serial number SI-10000 within IECEE CB Scheme. SIQ has been a full member of the CB scheme, as a certification body (NCB), since the end of 1993, when we also issued the f...
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Procedure for Certification of Medical Devices in Accordance with the Regulation (EU) 2017/745 on Medical Devices (MDR)
The path for the entry of a medical device to the market starts with an idea and leads through its production and testing to the eventual certification. It is recommended that the manufacturer contact the notified body already at the development s...
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SIQ is a notified body under the new Medical Devices Regulation
The medical device market accounts for more than a quarter of the global market. This is a sector that is constantly and rapidly evolving and requires constant adaptation by all stakeholders. The human population is aging, which is why rehabilitat...
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