La FDA admite, en documentos oficiales, que los test PCR no se desarrollaron con muestras del SARS COV-2 sino de material genético de la gripe estacional

También reconocen la manipulación de las cifras de positivos.

Documentos, más abajo, información de la abogada británica, Anna De Buiscuit.

Breaking news. share on all platforms: FDA document admits “Covid” PCR test was developed without isolated samples for test calibration, effectively admitting it’s testing something else.

A document just released by the U.S. Food and Drug Administration (FDA) openly admits that the infamous PCR test for the Wuhan coronavirus (Covid-19) was developed not with actual samples, but rather with what appears to be genetic material from a common cold virus.

From the document:

“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.”

Another revelation in the document is the admission by the FDA that test results are “pooled” together to produce numbers that are inaccurate.

You can

DOWNLOAD THE DOCUMENT HERE: https://www.fda.gov/media/134922/download

http://www.fda.gov (http://www.fda.gov/)

fda.gov (http://fda.gov/)

http://www.fda.gov (http://www.fda.gov/)

fda.gov (http://fda.gov/)

esta web esta abierta al debate, no al insulto, estos seran borrados y sus autores baneados.

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