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The explosion of new coronavirus tests that could help to end the pandemic
Researchers are scrambling to find other ways to diagnose the coronavirus and churn out millions of tests a week — a key step in returning to normality.
https://www.nature.com/articles/d41586-020-02140-8
‘Everyone tested positive’: Covid devastates agriculture workers in California’s heartland
https://www.theguardian.com/us-news/2020/aug/08/california-covid-19-central-valley-essential-workers
DECN MUST REGISTER GENVIROS WITH INDIA’S CDSCO.
Fauci: “chance of effective vaccine is 'not great'”
https://www.cnbc.com/2020/08/07/coronavirus-vaccine-dr-fauci-says-chances-of-it-being-highly-effective-is-not-great.html
BE VERY CAREFUL WITH THIS COMPANY; IT’S WAY TOO RISKY.
“EUA” CLEARED DEVICES ONLY SOLD FOR PANDEMIC DURATION. ONCE PANDEMIC IS LIFTED COMPANIES MUST OBTAIN FULL APPROVAL. DOESN’T SEEM LIKE DECN HAS THE CAPACITY TO SATISFY THEIR CLAIMS.
MADE MY $20,000. I’M OUT. EXTREMELY RISKY AND VERY DANGEROUS COMPANY WITH NOTHING TO SHOW AT ALL.
IF DECN HAD ANY PROTOTYPE THEY WOULD HAVE MADE A VIDEO.
Berman has yet to complete the feasibility studies. This means THAT DECN DID NOT submit any working prototypes the FDA OR CE MARK.
The EUA applications to amend and the saliva pre-EUA ARE NOT GOING TO BE CONCLUDED BY THE END OF SUMMER. BERMAN NEVER HAD ANY CONTROL OVER THE TIMELINES. I BELIEVE THEY HAVE THE TECHNOLOGY. BUT THE FDA CLEARANCE AND, EVEN, CE MARK APPLICATIONS ARE NOT ACCOMPANIED BY ANY PROTOTYPES.
If you bought low, hold for news.
REMEMBER: DECN shares are difficult to buy back.
THIS IS VERY SAD: https://www.worldometers.info/coronavirus/
New York erects COVID-19 checkpoints: https://www.reuters.com/article/us-health-coronavirus-usa-idUSKCN251281
IN 10.5 SECONDS, AT 95%+ FDA REQUISITE IS ALSO THE FASTEST.
CRUSHED ALL RESISTANCE GREEN: http://www.stockta.com/cgi-bin/analysis.pl?symb=DECN&cobrand=&mode=stock
The U.S. has the worst coronavirus outbreak in the world: 'The numbers don't lie,' Dr. Fauci says
PUBLISHED WED, AUG 5 2020 1:48 PM EDT
UPDATED AN HOUR AGO
https://www.cnbc.com/2020/08/05/dr-fauci-agrees-the-us-has-the-worst-coronvirus-outbreak-in-the-world-the-numbers-dont-lie.html
Bullish!!! BULL FLAG!!!!!
NO RESISTANCE, TOTAL SUPPORT; http://www.stockta.com/cgi-bin/analysis.pl?symb=DECN&cobrand=&mode=stock
Blown off the chart, VERY BULLISH, PARABOLIC: http://www.stockta.com/cgi-bin/analysis.pl?symb=DECN&cobrand=&mode=stock
DECN CREATED THE ONLY MULTI-VIRAL DETECTION TEST WITH A PATENTED “TBG SYSTEM,” THAT ELIMINATES THE NEED TO LYSE BLOOD HEMATOCRIT FOR VIRAL ISOLATION AND DETECTION. OUR TEST DOES NOT REQUIRE ANY LYSIS BUFFER, OR SURFACTANT AGENT AND COMPLETELY ELIMINATES HEMATOCRIT CROSS REACTIVITY WITH THE TBG-ADJUSTMENT FEATURE. THE GENVIRO SWIFT INCORPORATES THE
“TBG”TECHNOLOGY THAT ELIMINATES HEMATOCRIT INTERFERENCE. AND THE GENVIRO PROVIDES ACCURATE DIAGNOSTIC, LAB QUALITY RESULTS THAT ARE COMPARABLE TO EXISTING, SLOWER AND MORE COSTLY VIROLOGICAL LAB TESTS. OUR VIROLOGICAL DETECTION TEST PROVIDES RESULTS IN 10.5 SECONDS. OUR TEST PRODUCES THE FASTEST VIRUS DETECTION RESULTS IN THE WORLD.
IN ADDITION TO THE EMBEDDED TBG-TECHNOLOGY, DECN ALSO COMBINED THE MULTI-FUNCTIONALITY OF DETECTING VIRUSES THROUGH SALIVA, OR BLOOD IN THE SAME STATE OF THE ART TEST METER AND MULTI-FUNCTIONAL, PATENTED TEST STRIPS. DECN IS THE ONLY COMPANY IN THE WORLD THAT OFFERS THIS MULTI-FUNCTIONAL, VIRUS DETECTING TECHNOLOGY THAT MEETS AND SATISFIES THE USFDA REQUIREMENTS FOR IN VITRO VIRUS DETECTION PROTOCOLS AND CGMP REQUIREMENTS OF EUROPEAN CE MARKING.
LOOK: THERE’S MANY HOME DIAGNOSTIC TEST TYPES: https://www.google.com/search?client=safari&sa=X&bih=553&biw=375&hl=en-US&tbm=shop&ei=KdApX4TqDMql_Qab3IbYAg&q=home+diagnostic+tests&oq=home+diagnostic+test&gs_lcp=Cg5tb2JpbGUtc2gtc2VycBABGAAyAggAMgUIIRCrAjoECAAQGDoECAAQDToICAAQCBAHEB46BggAEAcQHjoECB4QClDgwwFYlIICYNmMAmgBcAB4AIABkQKIAYINkgEGMTQuMS4ymAEAoAEBqgESbW9iaWxlLXNoLXdpei1zZXJwwAEB&sclient=mobile-sh-serp
https://www.google.com/search?q=home+virus+tests&source=lmns&bih=553&biw=375&client=safari&prmd=sniv&hl=en-US&sa=X&ved=2ahUKEwjc25Lcu4LrAhUFIt8KHTEJBoMQ_AUoAHoECAAQAw
FDA APPROVED HOME TESTS: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm
There’s no reason to deny GENVIRO home kits, compared with available test kits: https://www.google.com/search?q=+home+test+kits&tbm=isch&ved=2ahUKEwjMvfe-l4LrAhVCZt8KHW5aCmYQ2-cCegQIABAC&oq=+home+test+kits&gs_lcp=ChJtb2JpbGUtZ3dzLXdpei1pbWcQDDICCAAyBggAEAgQHjIGCAAQCBAeMgYIABAIEB4yBggAEAgQHjoECCEQCjoECB4QCjoECAAQGFDL9wJYi4MDYPyOA2gAcAB4AIABigGIAfEHkgEEMTAuMpgBAKABAcABAQ&sclient=mobile-gws-wiz-img&ei=lakpX4wfwsz9Bu60qbAG&bih=553&biw=375&client=safari&prmd=sniv
CLOSE ABOVE .38, STRONG BUY ALERTS.
http://www.stockta.com/cgi-bin/analysis.pl?symb=DECN&cobrand=&mode=stock
EUA Authorized Serology Test Performance
https://www.fda.gov/medical-devices/coronavirus-disease-2019-covid-19-emergency-use-authorizations-medical-devices/eua-authorized-serology-test-performance
WE ARE NOT A SEROLOGY TEST. BUT THE FDA, 95% THRESHOLD REQUIREMENT FOR ANTIBODY CAN ONLY INDICATE VIRAL INFECTION, BY DETECTABLE ANTIBODIES THROUGH BLOOD SERUM CONVERSION - - “SEROCONVERSION.”
Viral infection or Virus must be present BEFORE DETECTABLE ANTIBODY LEVEL PRODUCTION. Rather than testing for antibodies, the GENVIRO SWIFT can detect the present virus in the early stage, BEFORE ANTIBODY PRODUCTION - - SEROCONVERSION.
NIH PROMOTED SLOW TESTING METHODS: https://www.nih.gov/news-events/news-releases/nih-delivering-new-covid-19-testing-technologies-meet-us-demand
DECN CREATED THE ONLY MULTI-VIRAL DETECTION TEST WITH A PATENTED “TBG SYSTEM” THAT ELIMINATES THE NEED TO LYSE BLOOD HEMATOCRIT FOR VIRAL ISOLATION AND DETECTION. OUR TEST DOES NOT REQUIRE ANY LYSIS BUFFER, AND COMPLETELY ELIMINATES HEMATOCRIT CROSS REACTIVITY WITH OUR PATENTED “TBG-ADJUSTMENT” FEATURE. THE GENVIRO SWIFT INCORPORATES THE “TBG”TECHNOLOGY THAT ELIMINATES ANY HEMATOCRIT INTERFERENCE. OUR EXCLUSIVE GENVIRO SWIFT PROVIDES HIGH THROUGHPUT, DIAGNOSTIC, LAB QUALITY RESULTS THAT ARE COMPARABLE TO EXISTING, SLOWER AND MORE COSTLY VIROLOGICAL TESTS. OUR VIROLOGICAL TEST PROVIDES RESULTS IN 10.5 SECONDS. OUR TEST PRODUCES THE FASTEST VIRUS DETECTION RESULTS IN THE WORLD WITH USFDA REQUIRED ACCURACY AND SENSITIVITY REQUIREMENTS.
IN ADDITION TO THE EMBEDDED TBG-TECHNOLOGY, DECN ALSO COMBINED THE MULTI-FUNCTIONALITY OF DETECTING VIRUSES THROUGH SALIVA, OR BLOOD IN THE SAME TEST METER WITH THE SAME MULTI-FUNCTIONAL, STATE OF THE ART, PATENTED TEST STRIPS. DECN IS THE ONLY COMPANY IN THE WORLD THAT OFFERS THIS MULTI-FUNCTIONAL, VIRUS DETECTING TECHNOLOGY THAT SATISFIES THE USFDA REQUIREMENTS FOR IN VITRO VIRUS DETECTION PROTOCOLS, WITH HIGH ACCURACY LEVELS AND USER FRIENDLY EFFICIENCY.
THE COMBINED FEATURES OF THE GENVIRO SWIFT RESULT IN A REVOLUTIONARY MULTI-FUNCTIONAL VIRUS TESTING METER THAT PROVIDES THE FASTEST, GROUND BREAKING RESULTS THAT IS EXCLUSIVELY PROVIDED BY DECN’s PATENTED DESIGN.
DECN PIONEERED THE ONLY ORIGINAL FASTEST MULTI-TEST.
DECN HAS ONLY 10.5 SECOND MULTI-TEST IN WORLD.
DECN IS THE FASTEST TEST IN THE WORLD.
CODX and DECN are the best patented tests in the world.