Malaria due to Plasmodium falciparum is probably the most important in
fectious disease in the tropical world. About 2000 million people live
in areas exposed to malaria and 300 million individuals are infected
every year. In Africa south of the Sahara alone, over 1 million childr
en die annually as a result of malaria. It is a difficult parasitic di
sease both to diagnose and control. It does not provide sterile immuni
ty even after long exposure periods. However, acquisition of partial i
mmunity allows over 60 per cent of individuals with long exposure to c
arry the parasite in their blood without symptoms, posing difficulties
for case definition, malaria attributable morbidity and deaths. Furth
er, it is extremely difficult to establish the extent to which malaria
has influence over the adverse outcome of other infectious disease li
ke measles and malnutrition. The complex life cycle of the parasite in
volving human and vector mosquitos as well as its allelic diversity an
d antigenic variations makes the development and implementation of eff
ective malaria control intervention problematic. It is now becoming ev
ident that multi-intervention approach may be the most appropriate way
of combating malaria in view of the increasing resistance of the para
site to antimalarial drugs as well as vector mosquitoes to insecticide
s. Malaria vaccines will therefore play a major role in future malaria
interventions. New malaria vaccine candidates will require testing in
malaria endemic countries. Sufficient sites for testing potential mal
aria vaccines must be prepared. In this paper we discuss the necessary
preparations required for field testing of malaria vaccines in tropic
al countries.