Device Specific Services
Safe devices for drug products
SAXOCON provides you with everything you need to test and document device compatibility with drug products in compliance with regulatory requirements.
Breathing gas pathways
SAXOCON can help you to plan, test, and document compliance with regulatory requirements and get your gas pathway products ready for CE Mark certification.
Safe in vitro diagnostics
SAXOCON helps 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.