SIQ
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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Social activities at SIQ: snapshots from the May picnic
This year again, we organized a traditional SIQ picnic in a lovely picnic place in the vicinity of Ljubljana. The picnic offered guided sports and an entertainment program with a competition in a team spirit. Seven teams competed in five disciplin...
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Complete Solutions for Medical Devices
We provide support to manufacturers of medical devices all the way from the idea and design to the placing of the device on the market with a variety of services – we train, test and certify. The comprehensive range of services...
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Complete solutions for Medical Devices in Accordance with the Medical Device Regulation
Medical devices play a key role in saving lives. They account for more than a quarter of the world market. This is a sector that is constantly and rapidly evolving and that requires constant adaptation of all stakeholders. The human population is ...
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7th International Safety & EMC Training Seminar
On May 12th and 13th, we successfully hosted our 7th International Safety & EMC Training Seminar at Hotel Kempinski in Portorož. More than 115 participants from 18 different countries joined us at the seminar, where they received an in...
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