Services for manufacturers of medical devices
The demands in the medical engineering industry are versatile: Standards (e.g. ISO 13485), statutory requirements (MPG, CFR Part 820) and your own quality requirements define the standards, which are inspected by authorities and through customer audits.
As your full service provider Testo I.S. is offering a cost-sensible implementation of your wishes and requirements in the fields of calibration, qualification, validation and quality assurance.
More assurance, better service: Our service portfolio