22 December 2021 — Global Research

By Prof Michel Chossudovsky

“The PCR is a Process. It does not tell you that you are sick”.

Dr. Kary Mullis, Nobel Laureate and Inventor of the RT-PCR, passed away in August 2019.

This misuse of the RT-PCR technique is applied as a relentless and intentional strategy by some governments to justify excessive measures such as the violation of a large number of constitutional rights, … under the pretext of a pandemic based on a number of positive RT-PCR tests, and not on a real number of patients.

.Dr. Pascal Sacré, Belgian physician specialized in critical care and renowned public health analyst.

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In the course of the next ten days (at the time of writing), the PCR test in the US will be declared invalid.

In a bombshell decision, the Centers for Disease Control and Prevention (CDC) has withdrawn the insidious PCR test as valid method for detecting and identifying SARS-CoV-2.

“After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only.”

In preparation for this change, CDC recommends clinical laboratories and testing sites that have been using the CDC 2019-nCoV RT-PCR assay select and begin their transition to another FDA-authorized COVID-19 test.

CDC encourages laboratories to consider adoption of a multiplexed method that can facilitate detection and differentiation of SARS-CoV-2 and influenza viruses. Such assays can facilitate continued testing for both influenza and SARS-CoV-2 and can save both time and resources as we head into influenza season. Laboratories and testing sites should validate and verify their selected assay within their facility before beginning clinical testing.

It has taken then almost two years to recognize that the PCR test is flawed and invalid.

This advisory by the CDC issued in July 2021 is to be enforced  in the course of the next couple of weeks leading up to the January 1st, 2022 deadline.

Will it be carried out?? Visibly there is no transition towards “another authorized Covid-19 test”.

What this means is a Mea Culpa. A tacit recognition by the CDC and the FDA that the entire data base generated by the PCR test is invalid.

Almost a year ago, in January 2021, the WHO questioned the validity of the PCR test which it had itself put forth as a means to detect and identify SARS-CoV-2 at the outset of the alleged pandemic in January 2020.

Several billion people in more than 190 countries have been tested (as well as retested) for Covid-19 using the PCR.test which is flawed and invalid.

We are talking about approximately 260 million alleged “Confirmed Covid-19 Cases” (PCR positives) Worldwide which constitute the data base of the alleged pandemic.

The pandemic is said to have resulted in more than 5 million Covid-19 related deaths.

These are nonsensical numbers.

And this data base is being used to justify the Covid-19 mRNA killer virus.

Bear in mind, in recent developments the PCR test is being routinely used to allegedly detect the variants including Delta and Omicron, which is an impossibility as well as a lie.