Evidence Now Emerging That Clinical Trials For mRNA Vaccines Were Compromised From The Beginning As Editor From British Medical Journal Sounds Alarm by Geoffrey Grider for Now The End Begins
The FDA only inspected 9 of the trial’s 150-plus sites before approving the vaccine. Just 9 sites. What about Moderna? FDA had over a year and inspected just one – ONE – of the trial’s 99 sites. How can FDA feel confident in the Moderna data based on a 1% sample?
The FDA only inspected 9 of the trial’s 150-plus sites before approving the vaccine. Just 9 sites. What about Moderna? FDA had over a year and inspected just one – ONE – of the trial’s 99 sites. How can FDA feel confident in the Moderna data based on a 1% sample?
Not to say we told you so, but we indeed told you so last year that, after all the smoke and mirrors of the man-made, gain of function pandemic started to settle down, the truth would begin to come out about what a sham the whole process really was. Now whistleblowers are beginning to make their voices known, and what they are telling us is downright terrifying if you were one of those people who agreed to receive the government injections.
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“And ye shall know the truth, and the truth shall make you free.” John 8:32 (KJB)
In 2020, everything was rushed and put through without much attention to detail, even the name of Trump’s vaccine campaign was entitled ‘Operation Warp Speed’. But there are some things that should not be rushed, a fine souffle is something that cannot be rushed, an untried and untested gene editing cocktail is also something that shouldn’t be rushed into production. As it turns out, the Pfizer and Moderna trials were in fact shams, with the shoddy protocols covered up and hidden from view as we were frightened into submitting to them. So go ahead, Facebook, give me another suspension for telling the truth, I couldn’t care less, the truth has set me free. You should try it some time.
Editor of the British Medical Journal tells the FDA about Serious Concerns over Pfizer Trial Data Integrity
FROM NAKED EMPEROR’S NEWS: Dr Doshi is an associate professor of pharmaceutical health at the University of Maryland School of Pharmacy, as well as a senior editor at the British Medical Journal. “His research focuses on the drug approval process, how the risks and benefits of medical products are communicated, and improving the credibility and accuracy of evidence synthesis and biomedical publications.”
In the most recent Food and Drug Administration (FDA) Vaccines and Related Biological Products Advisory Committee meeting in the US (6 April 2022), Peter dialled in to the Open Public Hearing Session. This is where members of the public can present their own information to the FDA. The committee was meeting to discuss considerations for the use of COVID-19 vaccine boosters and the process for COVID-19 vaccine strain selection to address current and emerging variants.
Peter told the FDA about Brook Jackson, a whistle-blower from Ventavia, which ran Pfizer’s vaccine trials. He discussed how unblinding of trial participants seems to have occurred and how this creates serious concerns about data integrity. Dr. Doshi also highlighted the lack of FDA inspection. A transcript of his comments is below.