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READ THE FDA’s OWN DOCUMENT FOR YOURSELF: “No quantified virus isolates of the 2019-nCoV were available for CDC use”

From the FDA directly and publicly available since July of 2021:
https://www.fda.gov/media/134922/download

An 80-page document titled: “CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel”

And what is the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel?

It is the official FDA documentation/instruction manual for the standard COVID testing method used throughout the pandemic.

On page 41 the document states:

“The analytical sensitivity of the rRT-PCR assays contained in the CDC 2019 Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel were determined in Limit of Detection studies. Since no quantified virus isolates of the 2019-nCoV were available for CDC use at the time the test was developed and this study conducted, assays designed for detection of the 2019-nCoV RNA were tested with characterized stocks of in vitro transcribed full length RNA (N gene; GenBank accession: MN908947.2) of known titer (RNA copies/μL) spiked into a diluent consisting of a suspension of human A549 cells and viral transport medium (VTM) to mimic clinical specimen.”

There are two important take-aways from the above text.

The first part of the second sentence:
“Since no quantified virus isolates of the 2019-nCoV were available for CDC use at the time the test was developed and this study conducted…”

Let that sink in.

And the second half of the the same sentence:
“…assays designed for detection of the 2019-nCoV RNA were tested with characterized stocks of in vitro transcribed full length RNA (N gene; GenBank accession: MN908947.2) of known titer (RNA copies/μL) spiked into a diluent consisting of a suspension of human A549 cells and viral transport medium (VTM) to mimic clinical specimen.”

In other words, apparently those involved in the testing and development had no actual COVID-19 virus to use during the development and testing of this method… so they CREATED an artificial “stand-in” for the COVID-19 virus that they used instead.

Anyone of sound mind should be able to understand the problem with what they are reading.

The entire COVID pandemic narrative has been reliant on the supposed detection of the virus via this official testing method. A testing method that was developed, tested and used worldwide minus the involvement of any actual COVID virus. By the FDA’s own admission via this now public document.

SIDE NOTE: On July 21, 2021 (ironically about the time the FDA document was released) The CDC announced that as of December 31, 2021 they will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization of this particular COVID testing method. The CDC provided this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternative testing methods: https://www.cdc.gov/csels/dls/locs/2021/07-21-2021-lab-alert-Changes_CDC_RT-PCR_SARS-CoV-2_Testing_1.html

RED PILL VINDICATION: During the very first episode of The Human Unleashed COVID-19 discussion series (recorded March 17th, 2020) Jeremy Ayres was already pointing out, asking and questioning if the virus had been isolated and shown to be pathogenic.

*Watch the video below:

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