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 […]

Emma Pedersen

Emma Pedersen (PhD) has been working with biological evaluation of medical devices for the past 11 years. She has extensive experience in testing of medical devices and GLP, from her previous work at RISE (Research Institutes of Sweden). She has special interest in the 3Rs, i.e, replacing animal testing with alternative testing methods. She is […]