Device Specific Services
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.
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.
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.
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.