An application of a quantitative PCR-based method was developed for the det
ection of human parvovirus B19 DNA. The procedure was characterised accordi
ng to guidelines for the validation of analytical procedures. Furthermore,
the reliability was demonstrated by the correct quantitation of samples of
an international collaborative study. This application might be useful for
studies focussed on removal and/or inactivation procedures of human parvovi
rus B19 as well as for general screening purposes of biological materials.