Medical Engineering Technologies is once more offering biocompatibility testing as part of its range of support services for medical device manufacturers.
This service covers biological safety testing according to ISO 10993, and consultancy on the testing required for CE Technical Files and FDA submissions, 510k and PMA.
Testing is carried out in ISO 17025-accredited laboratories in Europe, eliminating the common problem of getting development products through non-EU customs.
GLP studies are available according to FDA requirements.
