Great Lake Lab
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Syndromic testing

Workflow

Syndromic testing simplified

Clinical labs globally are facing ever greater demands on their time and resources. Diagnostic testing shouldn't be complicated. What if running a rapid diagnostic test was as easy as making your morning cup of coffee?

Everything you need in one easy-to-use cartridge

Set your clinical lab up for success with a streamlined syndromic test. The QIAstat-Dx Panels redefine ease-of-use with less than one minute hands-on time and a seamless sample to result workflow. Our innovative cartridge design includes all the reagents on board – ready to use. Your lab will easily adapt to molecular testing demands with minimal training and no precision pipetting required.

Maximize your impact on patient care with syndromic testing

With multiplex PCR testing, your lab can accelerate results and gain deeper insights compared to traditional methods. Empower your medical team with results delivered in time to be of clinical value in decision making.
  • Streamline your workflow

    With one molecular test that provides multiple results, you can reduce the number of low-plex, microscopy and culture tests ordered.

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  • Optimize laboratory operations

    With less hands-on time and minimal training required, you can process samples 24/7 without waiting to batch samples.

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  • Report fast results for at-risk patient populations

    With results available in about an hour compared to 2-3 days for some traditional methods, you can support patients in critical need of rapid results.

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  • Provide accurate results

    With improved sensitivity and specificity compared to some traditional methods, you can help improve patient management decisions.

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  • Reduce errors icon
    Streamline your workflow
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    Optimize laboratory operations
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    Report fast results for at-risk patient populations
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    Provide accurate results
Learn more about the benefits of syndromic testing
Reimagine your laboratory workflows with syndromic solutions.
Michelle Volk
“It became a very easy decision once we learned how sensitive and specific the QIAstat-Dx is and how easy it is to use.”
Michelle Volk, CEO and President of Great Lakes Labs, USA
Luca Sabatini, right profile
“The device is exactly what we need. It is so easy to use that after a short training, laboratory professionals in the medical team can easily operate it.”
Luca Sabatini, Medical Services Operator, Carnival Maritime, Italy
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Want to see more?
Get a closer look at the QIAstat-Dx Analyzer and QIAstat-Dx panels with our interactive demo.
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Get all the specs on QIAstat-Dx

Learn more about the features and specifications of the QIAstat-Dx Analyzer and QIAstat-Dx assays.

The QIAstat-Dx Analyzer is intended for in vitro diagnostic use.

The QIAstat-Dx Respiratory SARS-CoV-2 Panel is intended for in vitro diagnostic use.

  • This product has not been FDA cleared or approved, but has been authorized for emergency use by FDA under an EUA for use by authorized laboratories;
  • This product has been authorized only for the detection and differentiation of nucleic acid of SARS-CoV-2 from multiple respiratory viral and bacterial organisms; and
  • This 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.
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