Investigative journalist and author Jon Rappoport, after analyzing the CDC report "07/21/2021: Lab Alert: Changes to CDC RT-PCR for SARS-CoV-2 Testing", said their request to withdraw the Emergency Use Authorization for the PCR diagnostic test is not a sign that the CDC and the FDA have giving up on PCR testing but, instead, are preparing for an upgrade. The CDC's document admits it did not have a SARS-CoV-2 virus when it concocted the PCR test. They created a theoretical fabrication of it by using "contrived specimens" generated from a range of SARS-CoV-2 material sources. The CDC granted emergency authorizations to 59 different PCR tests, based on 59 varieties of "contrived specimens", in which no two were alike. The tests, of course, were useless. The CDC and FDA now are claiming they finally do have virus samples of SARS-CoV-2 from patients; that they now know what to look for, and that labs should start gearing up for new and improved PCR tests. They have yet to present the isolated virus to back their claims -GEG

The CDC has issued a document that bulges with interesting and devastating admissions.

The release is titled, "07/21/2021: Lab Alert: Changes to CDC RT-PCR for SARS-CoV-2 Testing." [1] It begins explosively:

"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. CDC is providing this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternatives."