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Unlock Expertise: Enroll in Our International Online Medical Device Compliance Training for 2024

Our courses, led by qualified experts with practical experience, are designed to cover the intricacies of medical device compliance. We've already announced training dates for the first half of 2024, offering you the opportunity to stay ahead in t...

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SIQ trainings for the global market – knowledge for trust

As SIQ has become increasingly recognized as an independent notified body for testing and certification of medical devices, there has been a growing interest in educational content about ensuring compliance of medical devices. Together with renown...

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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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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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