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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Training in the automotive industry

15. March 2022 Training

The automotive industry is one of the fastest-growing industries. It embodies the development of information and communication technology and technological development. It faces high research and development costs on a daily basis and incr...

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SIQ training programmes for the global market

11. October 2021 Training

We have enriched our international online training programmes with qualified lecturers and experts in MEDICAL DEVICES and

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