Service Swiss Medtech Expo 2023

MDR Readiness: We help you to get there!

Since 26.05.2021, the Medical Devices Regulation is fully applicable. Therefore, all processes related to design, industrialization, manufacturing and market surveillance must be aligned with the quality management system, which must be compatible with ISO 13485:2016 and/or USA QSR.

MDR-Conformity in 7 steps

We help you achieve your goal - Through our top expertise and a wealth of experience, we advise and support our global customers in updating and correcting their technical documentation. With this service, we ensure that processes along the entire lifecycle of medical devices are successfully accelerated and products remain safe. We stand for personal support, fast response times, adherence to deadlines and maximum flexibility.
Contact us now and learn more about our successful 7-step strategy to achieve full compliance of your technical documentation without detours.

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