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03:23 PM
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The PCR test is the Achilles' heel of the Coronavirus Psyop
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[quote:Lance Roseman From BC:MV80NTk3MTA0XzgzODM2NjQ0XzE3OUMwMDdC] [quote:Anonymous Coward 79687293:MV80NTk3MTA0XzgzODM2NTYwXzIwODExOEI5] [quote:Anonymous Coward 79687293:MV80NTk3MTA0XzgzODM2NTI2X0FEOEU3ODg4] Expose the PCR test! [b][b]Page 38[/b] https://www.fda.gov/media/134922/download[/b] [/quote] Thnx! Where's the URL with the link? [/quote] I mean, not the pdf directly, but the FDA page. The page where i can click to the pdf myself. That is what i asked for. Thnx for being awesome! [/quote] he optimum types of specimens to collect, and, during the course of infection, when these specimens are most likely to contain levels of viral RNA that can be readily detected. • Detection of viral RNA may not indicate the presence of infectious virus or that 2019-nCoV is the causative agent for clinical symptoms. • The performance of this test has not been established for monitoring treatment of 2019-nCoV infection. • The performance of this test has not been established for screening of blood or blood products for the presence of 2019-nCoV. • This test cannot rule out diseases caused by other bacterial or viral pathogens. Conditions of Authorization for the Laboratory The CDC 2019-nCoV Real-Time RT-PCR Diagnostic Panel Letter of Authorization, along with the authorized Fact Sheet for Healthcare Providers, the authorized Fact Sheet for Patients, and authorized labeling are available on the FDA website: https://www.fda.gov/MedicalDevices/Safety/EmergencySituations/ucm161496.htm Use of the CDC 2019-nCoV Real-Time RT-PCR Diagnostic Panel must follow the procedures outlined in these manufacturer’s Instructions for Use and the conditions of authorization outlined in the Letter of Authorization. Deviations from the procedures outlined are not permitted under the Emergency Use Authorization (EUA). To assist clinical laboratories running the CDC 2019-nCoV Real-Time RT-PCR Diagnostic Panel, the relevant Conditions of Authorization are listed verbatim below, and are required to be met by laboratories performing the EUA test. • Authorized laboratories1 will include with reports of the results of the CDC 2019-nCoV Real-Time RT-PCR Diagnostic Panel, all authorized Fact Sheets. Under exigent circumstances, other appropriate methods for disseminating these Fact Sheets may be used, which may include mass media. • Authorized laboratories will perform the CDC 2019-nCoV Real-Time RT-PCR Diagnostic Panel as outlined in the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel Instructions for Use. Deviations from the authorized procedures, including the authorized RT-PCR instruments, authorized extraction methods, authorized clinical specimen types, authorized control materials, authorized other ancillary reagents and authorized materials required to perform the CDC 2019-nCoV Real-Time RT-PCR Diagnostic Panel are not permitted. 2 • Authorized laboratories that receive the CDC 2019-nCoV Real-Time RT-PCR Diagnostic Panel must notify the relevant public health authorities of their intent to run the test prior to initiating testing. 1Authorized Laboratories: For ease of reference, the Letter of Authorization refers to “laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. § 263a, to perform high complexity tests” as “authorized laboratories.” 2If an authorized laboratory is interested in implementing changes to the CDC 2019-nCoV Real-Time RT-PCR Diagnostic Panel that are not in the scope (Section II) of this letter of authorization FDA recommends you discuss with FDA after considering the policy outlined in Immediately in Effect Guidance for Clinical Laboratories and Food and Drug Administration Staff: Policy for Diagnostics Testing in Laboratories Certified to Perform High Complexity Testing under CLIA prior to Emergency Use Authorization for Coronavirus Disease-2019 during the Public Health Emergency [/quote]
Original Message
This is taken from the
Instructions for Use Manual
provided by the CDC for the PCR test:
*
Detection of viral RNA may not indicate the presence of infectious virus or that 2019-nCoV is the
causative agent for clinical symptoms.
*
This test cannot rule out diseases caused by other bacterial or viral pathogens.
In short. The CDC is telling you that the PCR test can not confirm that you have an infection or that it is Covid.
The test is useless
.
Yesterday in Portugal, their court system deemed the PCR test "unreliable," and that is "unlawful to quarantine" people based on the unreliable PCR test.
Every system, framework, structure contains a weakness. A vulnerability that can be exploited. In the case of the Covid Psychological Terror Campaign. The weakness is the PCR test.
It exposes the entire thing as a fraud
.
Sure, there may be a nasty virus out there infecting some people. That's not the point. This is not about denying Covid. It's about exposing the fear and terror campaign being perpetrated with a faulty, unscientific test.
They could not get as far as they did without the fraudulent PCR test. There would be no justification for continued lockdowns and economic destruction.
The PCR test is the key to exposing and unraveling this campaign to destroy our lives. Share this information. Ask questions of doctors, politicians. Expose the PCR test!
Page 38
[
link to www.fda.gov (secure)
]
Portuguese Court Rules PCR Tests As Unreliable & Unlawful To Quarantine People
[
link to greatgameindia.com (secure)
]
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