The requirements of medical engineering are as varied as the products themselves. Standards such as
ISO 13485, statutory regulations (EU Directives, CFR Part 820, GMP) and our own quality requirements define the standards that are reviewed for compliance by authorities and customer audits.
As a full service provider, Testo Industrial Services will implement your requirements and requests
costsensitively in the fields of calibration, qualification, validation and GxP compliance.