The Medicines and Healthcare products Regulatory Agency (MHRA) has asked providers of laboratory-based COVID-19 antibody testing services using blood collected by a fingerprick to temporarily stop providing this service.
The measures will remain in place until home collection of this sample type has been properly assessed and validated for use with these laboratory tests, the regulator said in a statement on Friday (May 29).
This does not affect rapid, point of care tests or laboratory tests performed using blood taken from the vein, it noted.
The agency has recently updated its guidance on home antibody testing kits, to ensure that the public and industry have the latest information on the reliability of test results and what they mean.
Graeme Tunbridge, MHRA Interim Director of Devices, said: “Patient safety and public health are our main priorities and it is in the interests of everyone for antibody tests to be as reliable and meaningful as they can be.
“There are several UK providers of testing services who offer Covid-19 antibody testing using a fingerprick sample of capillary blood collected in a small container.
“We are asking all providers of laboratory-based Covid-19 antibody testing services using capillary blood collected by a fingerprick to temporarily stop providing this service until home collection of this sample type has been properly assessed and validated for use with these laboratory tests.”
Use of unvalidated sample types may lead to unreliable results and as such we are working closely with the service providers, laboratories and test manufacturers to resolve the regulatory and patient safety issues, he added.
