Solutions for SARS-CoV-2 Detection
We are here to help laboratories overcome their SARS-CoV-2 testing challenges so they can better address the world’s urgent public health concerns. We are working closely with laboratories around the world to deliver the nucleic acid isolation, automation, real-time PCR, antibody testing, and vaccine development solutions they need to rapidly respond to these challenges. Our top priority is to provide the technology and support to meet these needs.
Explore our SARS-CoV-2 Testing Products
COVID-19 Testing Lab-In-A-Lab Service
Increase your SARS-CoV-2 testing capabilities with the COVID-19 Lab-In-A-Lab™ testing solution, a full-service turnkey testing option embedded in your CLIA certified lab.
PerkinElmer New Coronavirus Nucleic Acid Detection Kit authorized under FDA EUA
The PerkinElmer New Coronavirus Nucleic Acid Detection Kit is a sensitive real-time RT-PCR test authorized under FDA EUA for the detection of COVID-19 in human oropharyngeal, nasopharyngeal, and anterior nasal swab samples.
PerkinElmer® SARS-CoV-2 Real-time RT-PCR Assay
The PerkinElmer® SARS-CoV-2 Real-time RT-PCR assay is CE-IVD marked and intended for in vitro diagnostic use in Europe. This assay provides reliable and high-quality results for the clinical detection of COVID-19 in human oropharyngeal swab, nasopharyngeal swab, bronchoalveolar lavage (BAL), sputum, plasma or serum samples.
PerkinElmer® GSP®/DELFIA® Anti-SARS-CoV-2 IgG Kit CE-IVD
The PerkinElmer® GSP®/DELFIA® Anti-SARS-CoV-2 IgG kit delivers qualitative detection of human IgG antibodies against SARS-CoV-2 in dried blood spots (DBS), plasma, and serum to identify individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection.
Automated, high-throughput processing of DBS is available with the GSP® instrument.
Manual processing of plasma and serum samples is available with the VICTOR2™ D instrument.
PerkinElmer® SuperFlex™ Anti-SARS-CoV-2 IgG Kit CE-IVD
The SuperFlex™ Anti-SARS-CoV-2 kit delivers fast, hands-free anti-SARS-CoV-2 IgG antibody detection using direct chemiluminescence technology. Up to 12 samples can be run in 15 minutes to quickly identify recent or prior infections.
Automated on the SuperFlex™ Chemiluminescent Immunoassay Instrument up to 48 samples can be processed per hour.
SARS-CoV-2 Test systems from EUROIMMUN a PerkinElmer Company
The complete package for SARS-CoV-2 virus and antibody detection.
Remote Services
Resolve instrument repairs faster and increase uptime. OneSource remote options do just that. Remote Support and Radian™ Remote Diagnostic services.
Webinar
Improve the Efficiency of Coronavirus Testing
This is a challenging time for laboratories working on the front lines of COVID-19 pandemic. In this webinar, we will describe how PerkinElmer is helping the community address this urgent public health concern. We will share details on immediately deployable solutions that can equip labs with viral nucleic acid isolation set up, extraction and detection to efficiently process thousands of tests every day.
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Blog Posts
Anterior Nasal Swabs for COVID-19 Testing
The FDA has authorized a new sample type, anterior nasal swabs, for use with some EUA authorized real-time RT-PCE assays for COVID-19 testing. Using anterior nasal swabs for SARS-CoV-2 testing offers many advantages over the typical sample types, human oropharyngeal and nasopharyngeal swab samples.
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Importance of Immunoassays for Coronavirus Control
On December 31, 2019, a pneumonia case in the Chinese city, Wuhan, with unknown pathological origin, was reported into the Chinese World Health Organization (WHO) office. By March 11, 2020, the virus had spread to 114 countries and had taken nearly 4,300 lives leading WHO to declare COVID-19 a global pandemic (WHO, 2020).
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How to Handle Inconclusive Samples with SARS-CoV-2 Real-Time PCR Tests
SARS-CoV-2 real-time reverse transcription polymerase chain reaction (RT-PCR) tests, can be inaccurate in two ways, as can all diagnostic assays. A false-positive result mistakenly identifies a person as infected, resulting in unnecessary quarantine and contact tracing. False-negative results are far more problematic because infected people may not isolate themselves and can infect others.
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Choosing a SARS-CoV-2 Real-Time RT-PCR Assay
Accurate detection of SARS-CoV-2 is critical for both patient treatments, as well as control of the COVID-19 pandemic. Many factors need to be considered when choosing a workflow to use for SARS-CoV-2 detection.
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Ensuring the Accuracy of your SARS-CoV-2 Testing Results
Accuracy of SARS-CoV-2 testing is critical when determining if someone is infected and needs to be quarantined and/or treated for a coronavirus infection. Real-time reverse transcription polymerase chain reaction (RT-PCR) assays are the tool of choice for determining if someone has an active viral shedding of SARS-CoV-2. RT-PCR assays reverse transcribe the viral RNA into DNA for amplification and subsequent identification of target regions.
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Significance & Difference between Target Regions for SARS-CoV-2 Testing
Severe acute respiratory syndrome coronavirus 2, or SARS-CoV-2, the virus responsible for the disease known as COVID-19, is now a global pandemic. This novel coronavirus was first observed in humans in December of 2019 and sequenced by multiple teams over the next month (Wu et al., 2020; Zhu et al., 2020; Chan et al., 2020).
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Helping Labs Test for COVID-19
The CDC limits IRR’s SARS-CoV-2 diagnostic reagent distribution to US state and/or local labs qualified to perform seasonal influenza surveillance testing and to local labs approved by their state public health laboratory to perform SARS-CoV-2 testing. Only CLIA facilities with appropriate equipment, training, and demonstration of testing proficiency can be considered.
Read MorePress Releases
PerkinElmer Releases New Dried Blood Spot Based COVID-19 Serology Test
WALTHAM, Mass.--(BUSINESS WIRE)--Jul. 21, 2020-- PerkinElmer, Inc. (NYSE:PKI), a global leader committed to innovating for a healthier world, today announced the launch of a dry blood spot (DBS) based test for SARS-CoV-2 IgG using its GSP®/DELFIA® platform, enabling processing of up to 5,000 samples per day.
Read MoreSonora Quest Collaborates with State and Health Care Leaders to Vastly Expand COVID-19 Testing Capacity in Arizona
July 9, 2020 PHOENIX — Governor Doug Ducey announced today a strategic collaboration with Sonora Quest Laboratories, the market share leader in diagnostics laboratory testing in Arizona, the Arizona Department of Health Services (ADHS) and PerkinElmer, Inc. (NYSE: PKI), a global leader committed to innovating for a healthier world, to expand testing in Arizona. The collaboration helps catapult COVID-19 diagnostic testing capacity well ahead of the significant demand in Arizona.
Read MoreGlobal Collaboration Establishes Wales’ National Covid-19 Testing Laboratory
An advanced laboratory dedicated to leading Wales’ national Covid-19 testing has been established in Cardiff, thanks to collaboration between Public Health Wales and one of the world’s leading diagnostics companies.
Read MoreFDA Provides Emergency Use Authorization to PerkinElmer for COVID-19 Testing
WALTHAM, Mass.--(BUSINESS WIRE)--Mar. 24, 2020-- PerkinElmer, Inc. (NYSE: PKI), a global leader committed to innovating for a healthier world, announced today that the U.S. Food and Drug Administration (FDA) has provided Emergency Use Authorization (EUA) for the Company’s New Coronavirus RT-PCR test.
Read MoreEUROIMMUN is one of first European manufacturers of diagnostic testing to provide CE-marked antibody detection systems to support COVID-19 diagnostics
The Anti-SARS-CoV-2 ELISAs for immunoglobulin classes A and G from EUROIMMUN, a PerkinElmer, Inc. company (NYSE:PKI), have received the CE mark and can now be applied to COVID-19 diagnostics. The PCR test EURORealTime SARS-CoV-2 has been submitted for CE mark.
Read MoreFDA Provides Emergency Use Authorization to PerkinElmer for Serological Test to Identify COVID-19 Antibodies
WALTHAM, Mass.--(BUSINESS WIRE)--May 5, 2020-- PerkinElmer, Inc. (NYSE: PKI), a global leader committed to innovating for a healthier world, announced today that the U.S. Food and Drug Administration (FDA) has provided Emergency Use Authorization (EUA) for EUROIMMUN’s (a PerkinElmer company) Anti-SARS-CoV-2 ELISA (IgG) serology test.
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