Barbara Musi BSc, PhD

Barbara brings 25 years of experience as a senior specialist in global support for biocompatibility strategy and toxicological risk assessment of products in development and sustaining products for dialysis systems and intensive care units at Baxter (previously Gambro AB), Lund Sweden. Most recently she worked for Altran as a senior consultant in toxicology and biocompatibility supporting MDR compliance.

Barbara has an MSc. in Neurobehavioral Sciences and a Ph.D. in Experimental Nephrology on the biocompatibility of peritoneal dialysis fluids in an animal model. Member of the ISO/TC 194 and ISO/TC 150, Biological evaluation of medical devices since 2001. She has large experience and expertise in vivo/in vitro models for regulatory biocompatibility studies, regulatory toxicology, and preclinical safety for the registration of medical devices and pharmaceuticals worldwide. Barbara has good communication skills and science dissemination through workshops, conferences, and lectures.