Explore our Comprehensive Training Programs Tailored for Laboratories and Inspection Bodies

Led by seasoned experts with hands-on experience, our courses delve into the intricacies of ISO/IEC 17025:2017 and ISO/IEC 17020:2012 requirements. Through engaging case studies and audit simulations, participants will gain the skills to autonomou...

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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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