Biocompatibility Testing of Medical Devices



Overview: Biocompatibility Testing of Medical Devices

The ISO 10993-1:2018 standard requires a structured biological evaluation plan within a risk management process. Learn which Biocompatibility, Microbiology, and Sterility Testing are most in demand and the services offered in our state-of-the-art facilities.

TÜV SÜD America can assist with the biological evaluation plan generation, toxicological risk assessment, and the conclusive biological evaluation report to help your device meet the risk requirements of the standard.

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