CDC withdraws support for PCR tests
Lab alert withdraws standing request to FDA to grant emergency use authorization for PCR tests to detect SARS-CoV-2
“The Centers for Disease Control and Prevention (CDC) will no longer recognize PCR tests as valid methods of diagnosing COVID-19 by the end of this year. The CDC announced in a lab alert on its website that it will be withdrawing its standing request to the Food and Drug Administration (FDA) to grant emergency use authorization for PCR tests to be used to detect SARS-CoV-2. The request, which was issued in February 2020, will be withdrawn on December 31, 2021, a move which signals that the CDC no longer approves of the use of PCR tests as valid diagnostic methods for COVID-19.
In the CDC’s own words: “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.”
The decision by the CDC, made in July 2021, comes as reports of false positive results to COVID tests have been increasing. Despite corporate media’s concerted efforts to discredit such reports, the climbing rate of false positive test results has gained international attention, most notably from real-life cases.
https://americasfrontlinedoctors.org/news/post/cdc-withdraws-support-for-pcr-tests/
Kary Mullis (the inventor of the PCR test) said “If you can amplify one single molecule up to something you can really measure, which is something you can do.…So that could be thought of as a misuse of it.”
I guess they are finally catching on – or – more likely – the other tests suit their goals better.
Yes — that is a concern. We know the PCR has NEVER worked for COVID but we also know that Gates has been busy buying up makers of other test processes. What will they bring out next to control the population and force digital passport implementation worldwide??
I like this quote on the Background of the Reference Panel for Comparative Data:
During the early months of the Coronavirus Disease 2019 (COVID-19) pandemic, clinical specimens were not readily available to developers of IVDs to detect SARS-CoV-2. Therefore, the FDA authorized IVDs based on available data from contrived samples generated from a range of SARS-CoV-2 material sources (for example, gene specific RNA, synthetic RNA, or whole genome viral RNA) for analytical and clinical performance evaluation.
Did you catch the 2 most important words there: “CONTRIVED SAMPLES”. THAT IS WHAT THEY USED TO JUSTIFY LOCKING DOWN THE WORLD! It that isn’t evil and criminal I don’t know what is. This is the premise that The Corona Investigative Committee in Germany headed by Reiner Fuellmich, ie, the false use of the PCR test to lock down the world, is using in his court case against those perpetuating this plandemic. Looks to me that the CDC is trying to avoid court cases.