Instructor

Barbara Musi

Barbara Musi (PhD) has 25 years of experience as 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. Standard Developer and member of the ISO/TC 194 and ISO/TC 150, Biological evaluation of medical devices since 2001.

She has extensive experience and expertise in in vivo/in vitro models for regulatory biocompatibility studies, regulatory toxicology and preclinical safety for the registration of medical devices and pharmaceuticals worldwide.D

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