The various mechanisms that contribute to the viral safety of therapeutics
prepared from human blood plasma are examined. The basic principles behind
the 2 most important mechanisms for viral safety, inactivation, and removal
are discussed, together with the main issues linked to manufacturing. Vali
dation of virus safety and protein integrity is considered. Currently avail
able methods for inactivetion and removal of viruses are reviewed, followed
by an overview of new and experimental methods that may have some promise
for the future. This review ends with a brief discussion of the impact frac
tionation pool size may have on product safety and the potential new threat
presented by contamination with prions. Copyright (C) 2001 by W.B. Saunder
s Company.