The Food and Drugs Authority (FDA) says it has neither registered nor recognized any rapid diagnoses test (RDT) kits for self-testing in the country. It said not even the World Health Organisation (WHO) had approved any RDT for use and, therefore, cautioned the public to be wary of any RDT kits. Speaking in an interview in Accra today, the Head of Medical Devices Department of the FDA, Mr Joseph Yaw-Bernie Bennie, said for now, only the Polymerase Chain Reaction (PCR) test was the recommended one and that was what the Noguchi Memorial Institute for Medical Research in Accra and the Kumasi Centre for Collaborative Research in Kumasi were using.
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He said currently, over 100 companies and institutions had approached the FDA to allow them to bring in RDTs from China, South Korea and other places with one of them requesting to be allowed for local mass production of the RDT kits in partnership with a foreign partner. “Since the outbreak of the pandemic in the country, a lot of people have made enquiries and the possibility of bringing in the RDT kits for testing on the COVID-19. Ordinarily, it is a good thing because the WHO is recommending that we should do mass testing.
“But we do not want to do test and give false positives and false negatives. So, there is the need to make sure that the tool you are using for testing is correct,” Mr Bennie explained.
He added that the COVID-19 was a novel virus which the scientist community was not very conversant with, “and almost everybody relies on good test cases.” Mr Bennie expressed concern that there was a lot of information being churned out, most of which was not correct, adding that Ghana was doing a lot of international collaboration to ensure that whatever the Ghanaian scientists were doing was good.
“Let me tell you that as of now that we are talking, WHO has not come out with any pre-qualified RDT that we can run with because it is not available as of now,” he said giving the assurance that if there was any RDT, Ghana would have been the first to go for them.