Norco

5555 Hamner Ave, Norco CA 92860

Appointment Required

Although all test results are reported, the State of California only counts PCR tests. If you would like your result to be counted by California and contribute toward Riverside County's testing numbers please select the Standard Molecular NAAT Test or the Rapid RT-PCR Test.

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Tests Available At This Site

Click on a test heading to see additional information

  • Rapid COVID-19 IgG/IgM Antibody $99
  • Standard Molecular NAAT (PCR or TMA) COVID-19 Test $125
  • Rapid COVID-19 Antigen Test $150
  • COVID-19 Antibody Test $160
  • Rapid COVID-19 Antigen + Flu Combo Test $175
  • Rapid RT-PCR COVID-19 Test (Best for Travel) $475

Rapid COVID-19 IgG/IgM Antibody Test

Results are generally reported within 60 minutes at most locations.

Assure COVID-19 IgG/IgM Rapid Test Device

  • IgG: This is the most common antibody. It’s in blood and other body fluids, and protects against bacterial and viral infections. IgG can take time to form after an infection or immunization.
  • IgM: Found mainly in blood and lymph fluid, this is the first antibody the body makes when it fights a new infection.

The Assure COVID-19 IgG/IgM Rapid Test Device, a test for the qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 (often referred to as COVID-19 or the novel coronavirus) in human venous whole blood (sodium EDTA), serum, plasma (sodium EDTA) and fingerstick whole blood.

The Assure COVID-19 IgG/IgM Rapid Test Device is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. At this time, it is unknown for how long antibodies persist following infection and if the presence of antibodies confers protective immunity

September 23, 2020 and the FDA guidance, “Policy for Diagnostic Tests for Coronavirus Disease-2019 during the Public Health Emergency” issued on March 16, 2020 (updated May 11, 2020). The

  • FDA issued this guidance to help accelerate the availability of novel coronavirus (COVID-19) tests developed by laboratories and commercial manufacturers during the public health emergency. This test has not been FDA cleared or approved; this test has been authorized by FDA under an EUA for use by laboratories certified under CLIA, that meet requirements to perform waived, moderate or high complexity test;
  • This test has been authorized only for the presence of IgM and IgG antibodies against SARS-CoV-2, not for any other viruses or pathogens;
  • This test 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 Act, 21 U.S.C. § 360bbb-3(b)(1),
    unless the authorization is terminated or revoked sooner.
  • Negative results do not preclude SARS-CoV-2 infection and should not be used as the sole basis for patient management decisions. The sensitivity of the EcoTest COVID-19 IgG/IgM Rapid Test Device early after infection is unknown. If acute infection is suspected, direct testing for SARS-CoV-2 is necessary.
  • Results from antibody testing should not be used as the sole basis to diagnose or exclude SARS-CoV-2 infection or to inform infection status;
  • Positive results may be due to past or present infection with non-SARS-CoV-2 coronavirus strains, such as coronavirus HKU1, NL63, OC43, or 229E.

Standard Molecular NAAT (PCR or TMA) COVID-19 Test

Results are generally reported within 2 – 5 days

Covid Clinic utilizes multiple independent laboratories to process specimens collected and multiple molecular tests in order to offer PCR or TMA testing on a consistent basis. The molecular NAAT PCR or TMA test will be one of the following three tests, but Covid Clinic is unable to guarantee which of the tests will be utilized for a specific sample:

Roche cobas SARS-CoV-2 RT-PCR

Hologic Aptima SARS-CoV-2 Assay

LabCorp COVID-19 RT PCR Test

Test Information

Covid Clinic is happy to offer COVID-19 PCR or TMA testing services. This testing meets the requirements for most travel restrictions; however, it is the purchaser’s responsibility to review any applicable travel restrictions prior to booking an appointment in order to ensure the service will meet the patient’s travel restriction requirement(s).

The specimen is collected by a nasal (anterior nares) swab. Please note that most travel restrictions require that a traveler’s test specimen IS COLLECTED within 48 to 72 hours upon arrival at destination. Results for the Standard Molecular NAAT (PCR or TMA) COVID-19 Test are generally reported within two to four days, but this delivery time is not guaranteed. If a patient needs their result delivered with a guaranteed turnaround time please see Covid Clinic’s Expedited Molecular NAAT (PCR or TMA) COVID-19 Test service offering.

Testing specimens collected at Covid Clinic are sent to third-party laboratories for processing. These laboratories may bill the patient’s insurance for their services. Covid Clinic strongly encourages all patients to provide any insurance information so patients may be able to avoid being billed directly by the third-party laboratory that processes the patient’s specimen. If a patient is uninsured, the third-party lab processing the specimen may attempt to collect public funding in lieu of billing the patient.

Rapid COVID-19 Antigen Test

Results are generally reported within 60 minutes

Quidel Corporation Sofia SARS Antigen FIA Test

Test Information

Covid Clinic is offering the Quidel Corporation Sofia 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 24 hours and delivered to the patient via email (with the individual’s consent).

COVID-19 Antibody Test

Roche Elecsys Anti-SARS-CoV-2 Total Antibody

Results are generally reported within two to five days

Test Information

The COVID-19 Antibody Test available at Covid Clinic test collection sites detects the presence of the SARS-CoV-2 (AKA COVID-19) antibodies in the patient’s blood. This test has Emergency Use Authorization from the FDA. Data published on the FDA’s website suggests this test has specificity of 99.8% and sensitivity of 99.5% when ≥ 14 days post PCR confirmation of prior COVID-19 infection. Results are generally available within two to five days, and will be communicated to the patient.

COVID Clinic’s service includes pre-test screening, specimen collection, presentation of results, and a post-result telemedicine consultation with a Covid Clinic healthcare professional.

Testing specimens collected at COVID Clinic are sent to third-party laboratories for processing. These laboratories will bill the patient’s insurance for their services. Covid Clinic strongly encourages all patients to provide any insurance information so patients may be able to avoid being billed directly by the laboratory processing the patient’s specimen. If a patient is uninsured the third-party lab processing the specimen may attempt to collect public funding in lieu of billing the patient.

COVID-19 Antigen + Flu Combo Test

Three tests in one! This test is recommended for all patients and especially those with symptoms

Tests for COVID-19, Influenza A, and Influenza B

Results are generally reported within 60 minutes

Test Information

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 60 minutes and delivered to the patient via email (with the individual’s consent).

Rapid RT-PCR COVID-19 Test

Results are generally reported within 24 hours

Satisfies most travel restriction requirements

Collected by anterior nares nasal swab (front of the nose only)

Test Information

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.

All testing administered by our testing partners, COVID Clinic

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Testing for Businesses, Organizations, and Events

Lifeline Health and testing facilitator COVID-Clinic are happy to offer COVID-19 related testing services to any business, organization, or event. To inquire, please email info@wearelifelinehealth.com with the dates you would like to begin testing, the estimated number of people to be tested, and the frequency of testing. Please include the business’s name, the primary contact’s phone number, and email address in the email subject line.