Evidence Now Emerging That Clinical Trials For mRNA Vaccines Were Compromised From The Beginning As Editor From British Medical Journal Sounds Alarm

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by Geoffrey Grinder, 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?

TRUTH LIVES on at https://sgtreport.tv/

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.

“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.

Hi, I’m Peter Doshi, thanks for the opportunity to speak. Hopefully you can see my title slide with my financial disclosures. For identification purposes, I am on the faculty at the University of Maryland and an editor at The BMJ. I have no relevant conflicts of interest and my comments today are my own.

Last November, The BMJ reported the disclosures of a whistle-blower named Brook Jackson, who worked for Ventavia, a contract research company that ran three of the clinical trial sites for Pfizer’s vaccine. Jackson alleged the company had falsified data, unblinded patients, employed inadequately trained vaccinators, and was slow to follow up on adverse events. She provided The BMJ with company emails, internal documents, text messages, photos and recordings of her conversations with company employees.

pfizer-moderna-mrna-vaccine-study-data-unblinded-fda

 This photo, for example, shows vaccine packaging materials that are only supposed to be seen by unblinded staff, just left out in the open.

And unblinding may have occurred on a far wider scale. Here you can see the document containing the instructions Ventavia staff were given to file each trial participant’s randomization and drug assignment confirmation sheet into each participant’s chart. This contained unblinded information.

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