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