Application deadline: 14 July 2014
The consultant will be expected to conduct a review of literature on the introduction of diagnostic testing into the private sector for diseases of public health importance other than malaria, map the landscape of international or regional efforts and the activities to harmonize regulation of in vitro diagnostic tests and develop the outline of a road map for implementing quality assured RDTs. He or she will also conduct a broad review of options for field-based quality control of malaria rapid diagnostic tests, review positive control well (PCW) specifications and investigate various potential options for future PCW use in national malaria programmes.
The consultancy is to start as soon as possible for a period of six months.
Full details can be found here.