Device Specific Services
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Safe devices for drug products
We provide you with everything you need to test and document device compatibility with drug products in compliance with regulatory requirements.
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Breathing gas pathways
We can help you plan, test, and document compliance with regulatory requirements and get your breathing gas pathway products ready for CE Mark certification.
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Safe in-vitro diagnostics
We help you ensure that your in-vitro diagnostic medical device complies with (EU) 2017/746 (IVDR) Annex I and is ready to be certified with a CE Mark.
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Safe stents and implants
We can help you get your stents and implants ready for CE Mark certification with our expert understanding of the ISO 10993-1 standard.