Datrend Systems Inc. has been assessed and registered by Intertek as conforming to the requirements of ISO13485:2016. The quality management system is applicable to design, manufacture and servicing of electronic equipment for medical applications and for the testing of medical equipment.
Datrend subscribes to the regulatory standards of CSA, UL, and the EU.
Products are designed and manufactured following the quality system principles of ISO and FDA QSR/cGMP.
Datrend’s Quality System is registered to ISO13485:2016.