• Working Hours - Mon - Fri: 9:00 - 17:00
What are you looking for?

UK GOVERNMENT APPROVED

UK Government Approved

PHE approval

The systematic evaluation of lateral flow assays during the COVID-19 pandemic was initiated at Oxford University as part of a UK collaboration with Public Health England (PHE).

PHE has only passed 3 Antigen Tests nationwide – with Healgen being one of them.

The test is also CE marked and manufactured in a US FDA (Food and Drugs Administration) approved facility.

Additional Certifications

The Healgen Rapid 15 minute Covid test also as the following certifications:

The data

Find out more about the Healgen COVID-19 Test

The Rapid COVID-19 Antigen Test is an in vitro immunochromatographic assay for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct nasopharyngeal (NP) swab from individuals who are suspected of COVID-19 by their healthcare provider. It is intended to aid in the rapid diagnosis of SARS-CoV-2 infections.

The technical details

Positive Percent Agreement (PPA): 97.3%
Negative Percent Agreement (NPA): 99.6%
Overall Percent Agreement (OPA): 98.9%