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Last Updated: 10/01/2020

Welcome to
Scion Lab Services

Scion Lab Services, LLC is a high complexity clinical testing facility licensed under the Clinical Laboratory Improvement Amendments of 1988 (“CLIA”), 42 U.S.C. Sections 263a, et seq. and the regulations promulgated thereunder, 42. C.F.R. Section 493, et seq. as well as the state of Florida, and accredited by the Commission on Office Laboratory Accreditation (“COLA”).

Scion Lab Services, LLC uses cutting edge equipment and technology to generate the most accurate lab testing results with a team of qualified professionals to bring you unparalleled service to exceed your expectations. Scion improves clinical outcomes with our diagnostic and preventative laboratory tests. When preventative laboratory tests are utilized appropriately the results can help reduce long term health care costs...

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Our Services

  • SARS-CoV-2 TESTING

    Our laboratory offers both IgG antibody and molecular testing for the detection of coronavirus (SARS-CoV-2).

    Molecular testing is performed on fluids from nasopharyngeal specimens. This real-time RT-PCR diagnostic panel is intended for diagnostic testing in symptomatic patients, suspected of exposure to COVID, or screening for exposure to asymptomatic individuals for COVID. The clinical criteria for testing using this panel includes those with clinical symptoms of COVID-19 and individuals know to have been in contact with a confirmed case of COVID-19. It is unknown when viral levels are at peak during an active infection, therefore, multiple samples may be required to detect the virus. More information about the appropriate use of testing can be found here: CDC Testing Guidance

    Antibody testing against SARS-CoV-2 is performed on serum usually after a patients has recovered from COVID-19 or a minimum of 10 days after initial exposure. This test is not used to confirm a clinical diagnosis. Having detectable antibodies to SARS-CoV-2 may mean a patient has some immunity, however, the World Health Organization states that having antibodies does not mean patients are completely protected from reinfection. Our analysis is performed on the Architect i1000sr instrument which utilizes chemiluminescent microparticle immunoassay technology (CMIA), providing results 24-48 hours after receipt of sample.
  • Pharmacogenomic Testing (PGX)

    Our PGX program uses the real-time PCR to provide information on variants in the DNA that affect how certain medications are absorbed, interact, broken down, or removed from our body. In the form of a comprehensive individualized report, based on the genetic results, we provide scientifically supported recommendations that are clinically relevant regarding which medications may be the most effective, what dosing is right and whether a patient is at risk for side effects.
  • Next Generation Sequencing for Inherited Cancer

    We provide hereditary cancer risk assessment testing using Next Generation Sequencing for detecting pathogenic genetic variants associated with an increased risk for developing a hereditary cancer. Genetic testing for inherited cancers involves sequencing specific genes to determine if pathogenic variants are present. Identifying individuals who have inherited a familial mutation may allow for earlier targeted or specialized screening procedures or treatment. Early detection may prevent death and other serious health problems from occurring.
  • Urine Toxicology

    We utilize enzyme immunoassay (EIA) technique to detect the presence of 8 drugs and 5 drug classes, as well as to determine urine specimen validity. With the combination of liquid chromatography and mass spectroscopy (LCMS-MS), we are able to uniquely identify over 80 drug analytes in urine, thereby enabling us to confirm initial screen results.
  • Chemistry

    We provide automated Serum Chemistry Testing that uses colorimetry, turbidimetry, latex agglutination, homogeneous EIA, and Indirect ISE technology. The chemistry testing we provide aids the physicians in providing specialized treatment protocols for patients in conjunction with toxicology and hematology results.
  • Hematology

    We provide automated in vitro diagnostic testing of a Complete Blood Count (CBC) and a 3-part automated differential white blood cell count. Physicians and health care providersare able to utilize the results from the CBC and differential to provide a complete treatment protocol along with the Toxicology and Serum Chemistry results on an individualized level.

Scion Lab Services will provide you with lab results that help you deliver a more personalized treatment and monitoring program. Our results can be forwarded to you or made available through our convenient web based portal within 24 - 36 hours following the receipt of each specimen.

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Accuracy is our Standard

Test result are verified to ensure the most accurate results possible

We give you Control

At Scion Labs, we customize every test panel based on each patient’s specific needs

Customized Delivery

We offer a number of options to our clients on how they want their test results delivered

We Keep Specimens Safe

Every specimen we receive is kept in constant check to ensure their delivery

We Keep Customers Happy

Our customer service and laboratory teams are available to help meet our customers’ needs

Fast Turnaround

The laboratory team at Scion Labs works hard to get you your test result within 24-36 hours

Licensed by

Accredited by

COLA Seal of Quality

If you Have Any Questions Call Us or Get In Touch