Employers are under more pressure than ever to protect the health and safety of their employees
Uncompromised on-site testing with the LumiraDx Platform delivers fast, accurate antigen testing. Rapidly identify potentially contagious spreaders on the spot, reducing the risk of a local outbreak & the potential impact on your operations, helping to build employee confidence
#Negative results do not rule out SARS-CoV-2 infection and should be considered in the context of an individual’s recent exposures, history and presence of clinical signs and symptoms consistent with COVID-19. Results should not be used as the sole basis for treatment or case management decisions, including infection control decisions
**Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status
SARS-CoV-2 Ab Test
The LumiraDx SARS-CoV-2 Ab Test is designed to be used in point of care settings to identify individuals who have antibodies to SARS-CoV-2
The LumiraDx SARS-CoV-2 Ab assay identifies antibodies to two viral regions that are primary targets for neutralising antibodies.
Knowing the COVID-19 antibody status of a workplace may allow employers and organisers to mitigate risk and make better informed choices on both micro and macro levels.View Test Page
We are focused on customer experience and dedicated to getting it right every time.Inquire now
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2: Report of the „Bundesamt für Gesundheit“ Switzerland 2020 (available upon request)
3: Kohmer et al., 2021. J Clin Med Jan 17;10(2):328.
4: Krüger et al., 2021 (https://www.medrxiv.org/content/10.1101/2021.03.02.21252430v1)
6: Drain PK, Ampajwala M, Chappel C, et al. A Rapid, High-Sensitivity SARS-CoV-2 Nucleocapsid Immunoassay to Aid Diagnosis of Acute COVID-19 at the Point of Care: A Clinical Performance Study. Infect Dis Ther. 2021;10(2):753-761.
7: Linares et al, Panbio antigen rapid test is reliable to diagnose SARS-CoV-2 infection in the first 7 days after the onset of symptoms, J Clin Virol. 2020 Dec; 133: 104659
8: Gannon C.K. Mak, Stephen S.Y. Lau, Kitty K.Y. Wong, Nancy L.S. Chow, C.S. Lau, Edman T.K. Lam, Rickjason C.W. Chan, Dominic N.C. Tsang, Evaluation of rapid antigen detection kit from the WHO Emergency Use List for detecting SARS-CoV-2, Journal of Clinical Virology, Volume 134, 2021, 104712, ISSN 1386-6532, https://doi.org/10.1016/j.jcv.2020.104712.
9: Young S, Taylor SN, Cammarata CL, Varnado KG, Roger-Dalbert C, Montano A, Griego-Fullbright C, Burgard C, Fernandez C, Eckert K, Andrews JC, Ren H, Allen J, Ackerman R, Cooper CK. 2021. Clinical evaluation of BD Veritor SARS-CoV-2 point-of-care test performance compared to PCR-based testing and versus the Sofia 2 SARS antigen point-ofcare test. J Clin Microbiol 59:e02338-20. https:// doi.org/10.1128/JCM.02338-20
10: Osterman, A., Baldauf, HM., Eletreby, M. et al. Evaluation of two rapid antigen tests to detect SARS-CoV-2 in a hospital setting. Med Microbiol Immunol 210, 65–72 (2021). https://doi.org/10.1007/s00430-020-00698-8
11. Labcorp EUA – Histogram of Cts, https://www.fda.gov/media/136151/download
12: Andrew Pekosz et al., Antigen-Based Testing but Not Real-Time Polymerase Chain Reaction Correlates With Severe Acute Respiratory Syndrome Coronavirus 2 Viral Culture, Clinical Infectious Diseases, 2021;, ciaa1706, https://doi.org/10.1093/cid/ciaa1706
Supporting healthier lives, for individuals, communities and wider society
Enabling responsive, personal relationships between patients and care teams.
Controlling and reducing costs to help ease pressure on healthcare budgets.