CDC:
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.
Visit the FDA website for a list of authorized COVID-19 diagnostic methods. For a summary of the performance of FDA-authorized molecular methods with an FDA reference panel, visit this page.
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.
This has been a money making scheme for the very beginning. The Ketchikan Hospital spent $500,000 for their PCR testing equipment. Now at the end of the year they will have to spent another half million dollars for another test that doesn't tell you if you have Corona, the cold or the Flu.
Last week, I reported the corporate media cover up for the "sudden deaths" this winter. I'm sure you've been seeing the 'sudden death' local obituaries too....In before, "so insensitive". No.
The Food and Drug Administration (FDA) asked a federal judge on Nov. 15 to give it until the year 2076 to fully release the documents in its possession tied to the approval of the Pfizer-BioNTech COVID-19 vaccine.
The FDA’s request was made in a filing as part of a Freedom of Information Act (FOIA) lawsuit by a medical transparency group. The government told the court it has 329,000 pages of documents responsive to the FOIA request and proposed releasing 500 pages per month to allow for redactions of exempt material. At that rate, the FDA would fully release the records in question in just under 55 years.
Children and pregnant mothers are being injected with mRNA unscientific shots that the developers refuse to release the 'science' on for 55 years. Please wake up. There are way too many coincidences and people dying 'suddenly' after getting their second or third mRNA shot to not see that there is serious medical malpractice happening.
On the heels of last weeks corporate media cover up, here are more articles explaining away the 'sudden deaths' that you've now seen more of after taking the shots than have died from corona. I truly have sympathy for people who are suffering now after getting these shots. However, you have a duty to show them the truth and wake them up.
I hate Big Pharma EXCEPT for Pfizer pic.twitter.com/lptKIwvUcf
— Ryan Long (@ryanlongcomedy) November 22, 2021
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