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$CEMI Top Institutional Holders
Holder Shares Date Reported % Out Value
Vanguard Group, Inc. (The) 855,245 Jun 29, 2021 2.99% 2,540,077
Segall Bryant & Hamill LLC 703,248 Jun 29, 2021 2.46% 2,088,646
Royce & Associates LP 491,453 Jun 29, 2021 1.72% 1,459,615
Penbrook Management, LLC 355,270 Jun 29, 2021 1.24% 1,055,151
Perkins Capital Management, Inc. 267,980 Jun 29, 2021 0.94% 795,900
Millennium Management LLC 251,869 Jun 29, 2021 0.88% 748,050
Blackrock Inc. 199,249 Jun 29, 2021 0.70% 591,769
Geode Capital Management, LLC 144,622 Jun 29, 2021 0.51% 429,527
Tibra Equities Europe Ltd 109,000 Jun 29, 2021 0.38% 323,730
Ameriprise Financial, Inc. 103,253 Jun 29, 2021 0.36% 306,661
https://finance.yahoo.com/quote/CEMI/holders?p=CEMI
One to hold on to, could bust out huge 500%+ in one day on that news IMO.
$CEMI
Easy calls, accumulated at this price range is a gift. They received EUA in the past they will get it again. FDA EUA approval will rock this to 8 dollars mark.
One of those that have a nice pop ahead IMO. All she needs is news and volume
$CEMI
$CEMI The current consensus among 2 polled investment analysts is to hold stock in Chembio Diagnostics Inc. https://money.cnn.com/quote/forecast/forecast.html?symb=cemi
$CEMI 20/50/200 Buying the Dip here, anyone else?
https://finviz.com/quote.ashx?t=CEMI&ty=c&p=d&b=1
Tiny float with volume it can go crazy. EUA within 30 days. I am loading up on the dip.
CEMI on watch
$CEMI
$CEMI Steady climb... The market is green again.
Breakout 2.70 let's go:)))
$CEMI The FDA has granted emergency use authorization to Chembio Diagnostics Inc's
CEMI partner LumiraDx's COVID-19 antibody test.
LumiraDx and Chembio had announced a partnership on March 12, 2020 to develop point of care COVID-19 antibody test.
The nod comes for LumiraDx SARS-CoV-2 Ab Test, a microfluidic immunofluorescence assay for the qualitative detection of total antibodies in whole human blood, plasma, or serum for indication of recent or prior infection.
Recently, the $CEMI received a $28 million order to supply DPP SARS-CoV-2 Antigen tests for delivery during 2021 in Brazil.
$CEMI CHEMBIO DIAGNOSTICS, INC. develops, manufactures, licenses and markets proprietary rapid diagnostic tests in the growing $5 billion point-of-care testing market. Chembio's two FDA PMA-approved, CLIA-waived, rapid HIV tests are marketed in the U.S. by a third party company. Chembio markets its HIV STAT-PAK line of rapid HIV tests internationally to government and donor-funded programs directly and through distributors. Chembio also has rapid tests for veterinary tuberculosis and chagas disease. In 2007 Chembio received a U.S. patent for its Dual Path Platform technology which has significant advantages over lateral-flow technologies. This technology is providing Chembio with a significant pipeline of business opportunities for the development and manufacture of new products based on DPP. Chembio is licensed by the U.S. Food and Drug Administration as well as the U. S. Department of Agriculture, and is certified for the global market under the International Standards Organization directive 13.485.
$CEMI Chembio Diagnostic Tweeted 'Biden has announced a new plan for COVID-19 Employers with 100+ workers will now require vaccines or weekly testing Chembio provides tests for Symptomatic & Asymptomatic serial testing, as well as multiplex COVID/Flu testing'
Chembio Announces EUA Submission for DPP Respiratory Antigen Panel
CEMI
+0.78%
Chembio Diagnostics, Inc.
Wed, September 22, 2021, 8:00 AM
In this article:
CEMI
+0.78%
Test Provides Simultaneous Detection of Flu A, Flu B, and SARS-CoV-2
HAUPPAUGE, N.Y., Sept. 22, 2021 (GLOBE NEWSWIRE) -- Chembio Diagnostics, Inc. (Nasdaq: CEMI), a leading point-of-care diagnostics company focused on infectious diseases, today announced the submission of an Emergency Use Authorization (EUA) application to the Food and Drug Administration (FDA) for the company’s DPP Respiratory Antigen Panel test system.
The DPP Respiratory Antigen Panel test system is designed to provide simultaneous, discrete, and differential detection of Influenza A, Influenza B, and SARS-CoV-2 antigens from a single patient sample using a simple nasal swab. The test system is expected to provide results in approximately 20 minutes and be read on Chembio’s DPP Micro Reader analyzer. The system is intended to enable appropriate clinical management of patients with suspected respiratory infections and to assist in the containment of COVID-19 cases during the flu season.
“Our DPP Respiratory Antigen Panel test system represents an additional differentiated offering among our COVID testing portfolio that can help clinicians at decentralized testing locations gain essential information about a patient’s infection status in only 20 minutes. COVID-19 infection rates are rising as we approach the flu season, and it is critical for clinicians to be able, at the point of care, to quickly triage respiratory infection patients with symptoms common to both COVID and flu infections and then administer the proper treatment regimen,” said Richard L. Eberly, Chembio’s President and Chief Executive Officer. “We believe this approach, as recommended by the U.S. Centers for Disease Control and Prevention, can save both time and resources. We are thankful for BARDA’s support and guidance throughout the development and evaluation of this test system.”
The DPP Respiratory Antigen Panel test system was developed with funds and support as part of a $12.7 million contract awarded by Biomedical Advanced Research and Development Authority (BARDA), part of the Office of the Assistant Secretary for Preparedness and Response at the U.S. Department of Health and Human Services. The contract also supports preparation of a submission to the FDA in pursuit of 510(k) clearance for the DPP SARS-CoV-2 Antigen test system.
About the DPP Rapid Test Platform
Chembio’s proprietary DPP technology platform provides high-quality, rapid diagnostic results in 15 to 20 minutes using a small drop of blood from the fingertip or alternative samples such as respiratory samples. Through advanced multiplexing, the DPP platform can detect up to eight, distinct test results from a single patient sample, delivering greater clinical value than other rapid tests. For certain applications, Chembio’s easy-to-use, highly portable, battery-operated DPP Micro Reader optical analyzer then reports accurate results in approximately 15 seconds, making it well-suited for decentralized testing where real-time results enable patients to be clinically assessed while they are still on-site. Objective results produced by the DPP Micro Reader reduce the possibility of the types of human error that can be experienced in the visual interpretations required by many rapid tests.
Chembio’s portfolio of DPP-based point-of-care tests with FDA regulatory approvals include the DPP HIV-Syphilis System (PMA approved), DPP HIV 1/2 Assay (PMA approved and CLIA waived), DPP Zika IgM System (510(k)), and DPP Ebola Antigen System (EUA). Additionally, DPP-based tests have received regulatory approvals from the World Health Organization, CE-Mark, Agência Nacional de Vigilância Sanitária (ANVISA), and other global organizations, where they aid in the detection and diagnosis of several other critical diseases and conditions.
All DPP tests are developed and manufactured in the United States and are the subject of a range of domestic and global patents and patents pending.
About Chembio Diagnostics
Chembio is a leading point-of-care diagnostics company focused on detecting and diagnosing infectious diseases, including COVID-19, sexually transmitted disease, and fever and tropical disease. Coupled with Chembio’s extensive scientific expertise, its novel DPP technology offers broad market applications beyond infectious disease. Chembio’s products are sold globally, directly and through distributors, to hospitals and clinics, physician offices, clinical laboratories, public health organizations, government agencies, and consumers. Learn more at www.chembio.com.
About the Project
This project has been funded in whole or in part with Federal funds from the Department of Health and Human Services; Office of the Assistant Secretary for Preparedness and Response; Biomedical Advanced Research and Development Authority, under Contract No. 75A50121P00012.
Forward-Looking Statements
Certain statements contained in the second and third paragraphs above are not historical facts and may be forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements regarding the intent, belief or current expectations with respect to the regulatory approval, distribution and sale of Chembio’s DPP Respiratory Antigen Panel test system, and the availability, timing, functionality and regulatory approval of the test systems. Such statements, which are expectations only, reflect management's current views, are based on certain assumptions, and involve risks and uncertainties. Actual results, events or performance may differ materially from forward-looking statements due to a number of important factors, and will be dependent upon a variety of factors, including, but not limited to, the following, any of which could be exacerbated even further by the continuing COVID-19 outbreak in the United States and globally: Chembio may be unable to anticipate or respond to changes in FDA regulatory requirements with respect to its proposed DPP Respiratory Antigen Panel point-of-care test system, or otherwise may be unable to obtain or maintain an EUA or other necessary regulatory approvals; Chembio’s development and commercialization efforts may not result in it successfully and timely developing and commercializing the DPP Respiratory Antigen Panel point-of-care test system; potential customers may not adopt point-of-care antigen systems to the extent expected by Chembio; Chembio business plans depend significantly upon, but Chembio has limited experience with, COVID-19 diagnostic tests; and Chembio may not be able to compete successfully with other companies that have developed, or develop in the future, COVID-19 antigen detection systems, some of which companies have substantially greater resources than Chembio. Chembio undertakes no obligation to publicly update forward-looking statements in this release to reflect events or circumstances that occur after the date hereof or to reflect any change in Chembio's expectations with regard to the forward-looking statements or the occurrence of unanticipated events. Factors that may impact Chembio's success are more fully disclosed in Chembio's periodic public filings with the U.S. Securities and Exchange Commission, including its Quarterly Reports on Form 10-Q for the quarterly periods ended March 31, 2021 and June 30, 2021, and its Current Report on Form 8-K filed with the Securities and Exchange Commission on July 19, 2021, particularly under the heading “Risk Factors” or similar headings.
DPP is Chembio’s registered trademark, and the Chembio logo is Chembio’s trademark. For convenience, these trademarks appear in this release without ® or ™ symbols, but that practice does not mean that Chembio will not assert, to the fullest extent under applicable law, its rights to the trademark.
Contact:
Philip Taylor
Gilmartin Group
415-937-5406
investor@chembio.com
There was a job fair poster on the comment section on webull. There was a number on there, I called it and there is a investors relations option 5. No one answered and I left a message the the called back within a couple hours. Really nothing more than what's been posted on already. I just thought it was cool the guy called back
$CEMI Infectious Disease Diagnostics Market worth $39.8 billion by 2026
Recently $CEMI received a $28 million order to supply DPP SARS-CoV-2 Antigen tests for delivery during 2021 in Brazil.
$CEMI First Rapid Test Approved in U.S. to Aid in Diagnosis of Both HIV and Syphilis from Single Patient Sample https://www.globenewswire.com/en/news-release/2020/10/02/2102866/21088/en/Chembio-Diagnostics-Receives-FDA-Approval-for-DPP-HIV-Syphilis-System.html
Biden has announced a new plan for COVID-19 Employers with 100+ workers will now require vaccines or weekly testing Chembio $CEMI provides tests for Symptomatic & Asymptomatic serial testing, as well as multiplex COVID/Flu testing
$CEMI CHEMBIO DIAGNOSTICS, INC. develops, manufactures, licenses and markets proprietary rapid diagnostic tests in the growing $5 billion point-of-care testing market. Chembio's two FDA PMA-approved, CLIA-waived, rapid HIV tests are marketed in the U.S. by a third party company. Chembio markets its HIV STAT-PAK line of rapid HIV tests internationally to government and donor-funded programs directly and through distributors. Chembio also has rapid tests for veterinary tuberculosis and chagas disease. In 2007 Chembio received a U.S. patent for its Dual Path Platform technology which has significant advantages over lateral-flow technologies. This technology is providing Chembio with a significant pipeline of business opportunities for the development and manufacture of new products based on DPP. Chembio is licensed by the U.S. Food and Drug Administration as well as the U. S. Department of Agriculture, and is certified for the global market under the International Standards Organization directive 13.485.
$CEMI 3rd Resistance Point 3.19
2nd Resistance Point 3.07
1st Resistance Point 2.84
Last Price 2.62
Delta variant surge causes COVID rapid test shortage in South Bend area
https://www.southbendtribune.com/story/news/2021/09/16/south-bend-covid-rapid-testing-delta-variant-vaccine-indiana-cases/8352273002/ $CEMI
Danm they shakeout a lot of tree today.
Nice entry here
Chembio Diagnostic $CEMI says today 'Biden has announced a new plan for #COVID Employers with 100+ workers will now require vaccines or weekly testing Chembio provides tests for Symptomatic & Asymptomatic serial testing, as well as multiplex COVID/Flu testing'
Covid19 Testing Mandates $CEMI
$$$$$$$$$$$$$$$$$$$$$$$$
Booooooooooooooooom
MARTA to begin mandatory COVID testing for unvaccinated employees
$CEMI https://www.11alive.com/article/news/health/coronavirus/marta-mandatory-covid-testing-unvaccinated-employees/85-78a76597-2235-454c-a98e-19c4a0f4ce64
UMD orders mandatory COVID-19 testing for four Cumberland Hall floors
$CEMI UMD orders mandatory COVID-19 testing for four Cumberland Hall floors $CEMI
COVID19 $CEMI 12-month price forecasts for Chembio Diagnostics Inc have a median target of 8.00, with a high estimate of 8.00 and a low estimate of 8.00. The median estimate represents a +201.89% increase from the last price of 2.65. https://money.cnn.com/quote/forecast/forecast.html?symb=cemi
Hopefully we see more contracts .. this one usually pops hard !
Chembio $CEMI Recent FDA Emergency Use Approval For Its #COVID19 Antibody Test. Recent To Ship $4M Of #WHO Qualified #HIV Test Kits To Ethiopia
Good morning all! Things look great today. Will CEMI start the short squeeze?
Take off tomorrow!
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