Make the right call
in COVID-19 care
Protecting the people in your care, on your staff and their families has never been more essential – especially when they may be at higher risk for life-threatening complications.
The BIOCARD® Pro COVID-19 Rapid Antigen Test detects multiple COVID-19 variants including the Omicron variant — be sure you have the accurate results you need to make the right decisions for those who depend on you.
When you are responsible for the healthcare of others, you need a COVID-19 test that is highly accurate and makes testing many easy and cost effective. Millions trust New Day’s BIOCARD Covid-19 test as it detects Omicron and Delta variants.
New Day’s BIOCARD COVID-19 accurately detects Omicron and Delta variants. Get fast, accurate results in just 10 minutes so you can protect yourself and your loved ones.
Breadth of Detection
Compared to PCR testing, our test had a PPA of 93.8% of Ct values below 35. By detecting positive cases even early and late in disease progression, the test offers a wider window in which to identify COVID-19.
Our test showed excellent sensitivity and specificity in detecting positive cases of COVID-19, including the Omicron and Delta variants, with 86.7% PPA and 100% NPA in symptomatic patients within the first 9 days of symptom onset.
Unique Test Design
Other tests simply dip or swirl the nasal swab in the buffer solution. Ours ensures high accuracy by leaving the swab in the solution – allowing it to process for two minutes before dripping the sample onto the proprietary test card.
Ready to Experience the Difference Yourself?
Bring Confidence to Any Care Setting
Speed is essential in any urgent care environment, and you need to know right away whether a patient is experiencing symptoms of COVID-19 or another illness. Our test delivers highly accurate results in just 10 minutes, so you can offer informed care plans sooner and keep your workflow moving.
You want to provide the best possible care to your patients, while reducing the chance of an outbreak among residents, visitors and staff. Our test provides the accurate results and early detection you need to make confident decisions that keep everyone safe and healthy.
Some of your patients may not be able to receive regular care, which makes it essential to diagnose and treat them in a single visit. Our test offers quick, highly accurate results without the need for on-site diagnostic equipment, so you can create a care plan right away.
How To Use the Test
Instructions For Use (IFU): Please carefully read and follow all instructions. It is important that you complete the test steps as accurately as possible to ensure reliable results.
For additional information about our test, view our frequently asked questions.
CE Mark for Professional use.
This item is currently not available for sale in the USA until FDA authorized. This page is made available for informational purposes only.
*PPA = positive percent agreement
**NPA = negative percent agreement
†Ct values = cycle threshold value. The higher the Ct, the more PCR cycles it took to identify the presence of the antigen. This means that a higher Ct indicates lower viral loads.
- This product has been authorized by the FDA under an Emergency Use Authoization (EUA)
- This product has been authorized only for the detection of proteins from SARS-CoV-2, not for any other viruses or pathogens.
- The emergency use of this product is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostics for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 360bbb3(b)(1), unless the declaration is terminated or authorization is revoked sooner.