Computational Modeling and Simulation of Medical Device Biocompatibility: Focus on Thrombosis Modeling

Computational Modeling and Simulation of Medical Device Biocompatibility: Focus on Thrombosis Modeling

Assessing thrombosis potential is essential to establishing the biocompatibility of blood-contacting medical devices. Computational fluid dynamics (CFD) has proven to be a useful complementary tool for understanding mechanical sources of blood damage such as shear stress, exposure time, and flow recirculation. In an effort to understand the applicability of thrombus modeling for device development and regulatory review, an industry round-robin study was carried out by the MDIC Blood Damage Working Group. This webinar will review the results of this round-robin study and discuss future directions for this work.

Learn more about the Computational Modeling & Simulation Program a MDIC

Presented By:

Brent Craven, PhD

Research Scientist & Program Manager (Acting), Credibility of Computational Modeling and Simulation Program, OSEL, CDRH, FDA

Jithesh Veetil, PhD

PhD, Senior Program Director, Digital Health & Technology, MIDIC

Kurt Svihla

Lead Engineer

Marc Horner

Distinguished Engineer

Koohyar Vahidkhah, PhD

Distinguished Engineer, Advanced Engineering Services