Covid-19 Testing near
Ontario Airport

All of Covid Clinic’s antigen test offerings utilize tests that have received emergency use authorization from the FDA.

For Quidel’s Sofia SARS Antigen FIA Test and Luminostics Clip COVID Rapid Antigen Test, the specimen is collected by a lower nasal swab (anterior nares). The cotton swab does not need to be inserted far into the nose, and is rotated in a circle around the entire inside edge of each nostril at least three times. Results are generally available within 1 hour and delivered to the patient via email (with the individual’s consent).

For Access Bio’s CareStart COVID-19 Antigen Test, the specimen is collected by a lower nasal swab (anterior nares). Results are generally available within 1 hour and delivered to the patient via email (with the individual’s consent).

The price for the Rapid COVID-19 Antigen Test Service includes payment for medical oversight, collection site infrastructure, performance of sample collection, test materials, test processing, information systems, result reporting, result delivery, other ancillary services, and other costs incurred by COVID Clinic.

Quidel Corporation Sofia SARS Antigen FIA Test

• Test Information
• Fact Sheet for Patients
• EUA Letter from the FDA

Access Bio, Inc. CareStart COVID-19 Antigen Test

• Test Information
• Fact Sheet for Patients
• EUA Letter from the FDA

Covid Clinic is offering the Quidel Corporation Sofia 2 FLU + SARS Antigen FIA Test. This test has received an emergency use authorization from the FDA.

The specimen is collected by a nasal swab. The cotton swab does not need to be inserted far into the nose, and is rotated in a circle around the entire inside edge of each nostril at least three times. Results are generally available within 1 hour although result time may vary from location to location.

The price for the COVID-19 Antigen + Flu Combo Test Service includes payment for medical oversight, collection site infrastructure, performance of sample collection, test materials, test processing, information systems, result reporting, result delivery, other ancillary services, and other costs incurred by COVID Clinic.

• Test Information
• Fact Sheet for Patients
• EUA Letter from the FDA
• FAQ

Covid Clinic, Inc. is offering the Abbott ID Now COVID-19 Assay performed on the ID NOW Instrument. This test is a rapid molecular in vitro diagnostic test utilizing an isothermal nucleic acid amplification technology intended for the qualitative detection of nucleic acid from the SARS-CoV-2 viral RNA in direct nasal swabs. The ID Now COVID-19 Assay has received Emergency Use Authorization (EUA) from the FDA.

Many travel restrictions require a molecular or NAAT test be conducted prior to arrival. Abbott’s ID Now COVID-19 test may satisfy these requirements; however, it is the purchaser’s responsibility to verify the test will be accepted for travel prior to purchase.

To collect a nasal swab sample, carefully insert the swab into the nostril exhibiting the most visible drainage, or the nostril that is most congested if drainage is not visible. Using gentle rotation, push the swab until resistance is met at the level of the turbinates (less than one inch into the nostril). Rotate the swab several times against the nasal wall then slowly remove from the nostril. Using the same swab, repeat sample collection in the other nostril.

The price for the Rapid COVID-19 Molecular NAAT Test Service includes payment for medical oversight, collection site infrastructure, performance of sample collection, test materials, test processing, information systems, result reporting, result delivery, other ancillary services, and other costs incurred by COVID Clinic.

Abbott ID Now COVID-19 Assay

• Test Information
• Fact Sheet for Patients
• EUA Letter from the FDA

The Rapid RT-PCR COVID-19 Test is a molecular, in vitro diagnostic test utilizing end point reverse transcriptase polymerase chain reaction (RT-PCR) and lateral flow technologies for the qualitative, visual detection of the coronavirus SARS-CoV-2 viral RNA. The four steps utilized to perform the test are lysis of the virus, reverse transcription of viral RNA to cDNA, nucleic acid amplification, and detection.

The Rapid RT-PCR COVID-19 Test has been released under FDA Emergency Use Authorization (EUA) for the detection of nucleic acid from SARS-CoV-2 (the virus responsible for COVID-19 infection), and can be used in applications that require molecular/ RT-PCR testing. Please consult your state health department for additional information regarding specific uses (such as pre and post travel requirements). Many travel restrictions require a RT-PRC, molecular, or NAAT test be conducted prior to arrival at the destination. The Rapid RT-PCR COVID-19 test satisfies most travel requirements; however, it is the purchaser’s responsibility to verify the test will be accepted for travel prior to purchase.

The price for the Rapid RT-PCR COVID-19 Test Service includes payment for medical oversight, collection site infrastructure, performance of sample collection, test materials, test processing, information systems, result reporting, result delivery, other ancillary services, and other costs incurred by COVID Clinic.

The RT-PCR COVID-19 Test has been released under FDA Emergency Use Authorization (EUA) for the detection of nucleic acid from SARS-CoV-2 (the virus responsible for COVID-19 infection), and can be used in applications that require molecular/ RT-PCR testing. Please consult your state health department for additional information regarding specific uses (such as pre and post travel requirements). This test is an RT-PCR, molecular and NAAT test which satisfies most travel requirements; however, it is the purchaser’s responsibility to verify the test will be accepted for travel prior to purchase. Please note that most travel restrictions require that a traveler’s test specimen IS COLLECTED within 72 hours prior to arrival at a destination.

The price for the Expedited RT-PCR COVID-19 Test Service includes payment for medical oversight, collection site infrastructure, performance of sample collection, test materials, test processing, information systems, result reporting, result delivery, other ancillary services, and other costs incurred by COVID Clinic.

• Test Information
• Fact Sheet for Patients
• EUA Letter from the FDA

• Test Information
• Fact Sheet for Patients
• EUA Letter from the FDA

• Test Information
• Fact Sheet for Patients
• EUA Letter from the FDA