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FDA document admits that the “Covid” PCR test was developed with no isolated samples for test calibration, thereby admitting that it tests something else.
A document just released by the U.S. Food and Drug Administration (FDA) openly admitted that the infamous PCR test for the Wuhan coronavirus (Covid-19) was not developed using real samples, but using genetic material that seems to come from a cold virus.
The FDA document clearly states that common seasonal flu genetic material was used as a test marker in the PCR test kits because authorities knew that many people would test “positive” for it, so they could use these results to to make the “Covid” claim.
It is a bit of a tedious read to read, but see for yourself and spot the obvious fraud. There is no reliable test that exactly determines the presence of SARS-CoV-2.
From the document:
“Since no quantified virus isolates of the 2019-nCoV were available for the CDC at the time the test was developed and this study was carried out, tests for the detection of the 2019-nCoV RNA with characterized stocks of in vitro transcribed full-length RNA (N- Gen; GenBank access: MN908947.2) with a known titer (RNA copies / µL) which was added to a diluent consisting of a suspension of human A549 cells and a viral transport medium (VTM) in order to mimic a clinical sample. “
Another revelation in the document is the FDA’s admission that test results are “pooled” to get inaccurate numbers.
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