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

Share on facebook
Share on twitter
Share on linkedin
Share on whatsapp
Share on email

Related courses to Barbara Musi

Biological evaluation of Medical Devices

Nov 22
- Nov 23, 2021
Copenhagen, Denmark
Toxicology, biological assessments

The role of GLP in medical device biocompatibility testing

Aug 25



For your best experience are we using cookies on this website.