The Hough Covid-19 Test is currently pending FDA EUA approval for over the counter in the USA

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About Hough

Hough Pharma's Antigen Rapid Test Kit

SARS-COV-2 Fluorescence Immunochromatography

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Provides results within 15 minutes.

Detects COVID-19 in people with or without symptoms.

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Secure Reporting

Our Antigen Rapid Test Kit - SARS-COV-2 Fluorescence Immunochromatography tests are supported by our BOH-180 analyzer system that records and reports results to state health authorities and an individual worker's eHealth records (subject to respective company policies and procedures)

The system can be automatically set to send results directly to an individual's phone to store to in their Apple or Google Wallets for use as needed.

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The portable system is plug-and-play and the only one of its kind currently available in the Australian market.

Download: BOH-180 system info

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Personalized cloud powered Certified help map COVID-19, slow the spread and save lives.

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How it works

Rapid antigen testing is a screening tool that can help detect COVID-19 in people with or without symptoms of COVID-19. Rapid antigen testing involves a nasal swab ( using a small cotton bud).
Then Placed into a chemical solution. The result is available in 15 minutes.

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This test does NOT determine if you had COVID-19 in the past or if you have immunity.

Do not use this test as the only guide to manage your illness.
Please consult a healthcare professional if your symptoms persist or become more severe or if you are concerned at any time.

Download: BOH-180 QRI

Contact Us

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COVID-19

Home test

Where to buy

Hough COVID-19 Home Test is available to those who need it most—working with commercial partners to ensure distribution to retail stores across Australia.

Hough Pharma's Rapid Antigen Home Test is listed on the Australian Register for Therapeutic Goods (ARTG number 345031)

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© 2021 Hough Pharma

The Hough COVID-19 Home Test Has not been FDA cleared or approved but is pending authorization by the FDA under an emergency use authorization. This product is only for the detection of proteins from SARS-CoV-2. Not for any other viruses or pathogens. and only for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for the detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug, and Cosmetics Act, 21 USC § 360bbb-3(b)(1) unless the declaration is terminated or authorization is revoked sooner.

Negative test results do not exclude infection with COVID-19 (so face masks, social distancing and good hygiene practice must be maintained);