Presents an up-to-date treatment of research strategies, clinical
and commercial developments, and regulatory and economic issues
pertaining to the formulation of effective and safe red blood cell
substitutes. The text examines regulatory and socioeconomic aspects
of blood substitute products, and global tranfusion practices from
the perspective of blood banks and the US Food and Drug
Administrations. It also includes the mechanisms of action and
consequences of blood substitute administration.
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