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Explore our core diagnostic menu and see what's coming next
Get the right diagnosis the first time
We’re committed to helping healthcare workers like you navigate the challenges of diagnosing infectious diseases. That’s why we’ve developed an easy-to-use, automated diagnostic testing system that can help eliminate the guesswork and make your job easier. Our tests use multiplex PCR technology – also known as syndromic testing – that can quickly survey many different pathogens in a single patient sample. With syndromic testing, you get the answers you need, when you need them. And your patients get better care, faster.
Latest insights – webinars, stories and more
Voices from the field – how medical professionals are using syndromic diagnostics
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Celestin Alexis Agbessi, M.D., Bichat-Claude Bernard Hospital, Paris
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Michelle Volk, CEO and president of Great Lakes Labs, Indiana, USA
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Joshua Arant, Founder and Chief Operations Officer, Mako Medical
Featured – resources for infectious disease diagnostics
References
- Yalamanchili H, et al. (2018) Gastroenterol Hepatol, 14(11):646-652
- Binnicker M. Multiplex. (2015) J. Clin Microbiology, 53(12):3723-3728
- Macfarlane-Smith L, et al. (2018) Gastrointestinal Infections, 34(1):19-2
- Echavarria M, et al. (2018) J Clin Virol, 108:90–95
- Beal S G, et al. (2018) J Clin Microbiol, 18;56(1)
- Bouzid D, et al. (2020) J Hospital Infection, 337-338
- Iroh Tam PY, et al. (2017) Children (Basel), 4(1)
- Zhu et al. (2018) Clin Pediatr, 58(2): 185-190
- Martinez RM, et al. (2016) Clinical Virology Symposium, Poster #C-368
*Some features require a QIAstat-Dx Connectivity plan. Flexible plans are available to meet your lab’s needs.
The QIAstat-Dx Viral Vesicular Panel is for research use only. The QIAstat-Dx Viral Vesicular Panel is run on the QIAstat-Dx Analyzer.
The QIAstat-Dx Analyzer 1.0, QIAstat-Dx Rise, QIAstat-Dx Respiratory SARS-CoV-2 Panel and QIAstat-Dx Gastrointestinal Panel 2 are intended for in vitro diagnostic use.
The QIAstat-Dx ME Panel is indicated as an aid in the diagnosis of specific agents that cause meningitis and/or encephalitis, and results must be used in conjunction with other clinical, epidemiological, and laboratory data. Results from the QIAstat-Dx ME Panel are not intended to be used as the sole basis for diagnosis, treatment, or other patient management decisions. Positive results do not rule out co-infection with organisms not included in the QIAstat-Dx ME Panel. The agent or agents detected may not be the definite cause of the disease. Negative results do not preclude central nervous system (CNS) infection.
The QIAstat-Dx ME Panel is intended for in vitro diagnostic use by laboratory professionals only.
Product availability may differ from country to country based on regulations and approvals. Contact your country representative for further details.
For up-to-date licensing information and product-specific disclaimers, see the respective QIAGEN kit instructions for use or user manual. QIAGEN instructions for use and user manuals are available at www.qiagen.com or can be requested from QIAGEN Technical Services (or your local distributor).