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USA: Breaking News - Fraud allegations against Pfizer

USA: Breaking News - Fraud allegations against Pfizer
  • 16 February 2022

This is an interesting legal action brought against Pfizer and their contractor Ventavia in the United States District Court for the Eastern District of Texas Beaumont Division. This legal action was originally lodged in court on 1 August 2021 but the original complaint was only unsealed by the court on 10 February 2022.

This legal action appears to form part of an unfair dismissal claim brought by Brook Jackson against Ventavia. (We may be wrong, but its just our observation)

 

However the 81 pages complaint puts the spotlight on events leading to the allegation that fraud took place during the initial clinical trials that led to FDA’s emergency use authorization of the Pfizer vaccines in the USA.

 

Background to the complaint

Extract from the original document that you can download from the attachment section of this page.

 

“ … Developing a safe and effective vaccine against the novel Coronavirus (“COVID-19”) was a matter of urgency. But that urgency does not excuse cutting corners in clinical trials, wasting taxpayer dollars, violating federal regulations, and possibly endangering Americans’ health.

Defendants Pfizer Inc., Icon PLC, and Ventavia Research Group, LLC (collectively, “Defendants”) conducted a clinical trial to test one of the COVID-19 vaccine candidates.

In the race to secure billions in federal funding and become the first to market, Defendants deliberately withheld crucial information from the United States that calls the safety and efficacy of their vaccine into question. Namely, Defendants concealed violations of both their clinical trial protocol and federal regulations, including falsification of clinical trial documents. Due to Defendants’ scheme, millions of Americans have received a misbranded vaccination which is potentially not as effective as represented. The vaccine’s U.S. Food and Drug Administration (“FDA”) authorization resulted from a deeply flawed clinical trial that violated FDA regulations. Defendants have profited from the COVID-19 pandemic at the expense of the United States and its citizens by abusing the scientific process.

BioNTech SE (“BioNTech”) and Defendant Pfizer Inc. (“Pfizer”) co-developed a messenger RNA vaccine against COVID-19. After a reportedly successful Phase 1 clinical trial, Pfizer entered into a contract with the United States Department of Defense (“DoD”), under which DoD would purchase 100 million doses of the vaccine for $1.95 billion following FDA approval or Emergency Use Authorization (“EUA”). Pfizer and BioNTech became co-sponsors of Phase 2 and 3 clinical trials for their vaccine, aiming for FDA approval or EUA status.

Pfizer delegated management of the clinical trial to subcontractor Defendant Icon PLC (“Icon”), an Irish clinical research organization. Icon was tasked with oversight of over 160 test sites worldwide, ensuring trial protocol compliance, and ensuring reporting of required information. This includes oversight of Serious Adverse Event (“SAE”) reporting, which is required by the trial protocol and federal regulations. Pfizer remained responsible for managing and quality checking all data for the entire clinical trial, per the trial’s protocol.

Defendant Ventavia Research Group, LLC (“Ventavia”) was contracted by Pfizer to provide three Phase 3 test sites for the vaccine trial in Houston, Fort Worth, and Keller, Texas. Ventavia ultimately enrolled about 1,500 clinical trial patients. Ventavia employed Relator Jackson as a Regional Director. She was tasked with overseeing site management, patient enrollment, quality assurance completion, event reporting, corrective action plan creation, communication with management, and staff training completion at the Keller and Fort Worth sites.

Pfizer, aiming for the title of “first successful COVID-19 vaccine,” pushed Ventavia to enroll as many patients as possible in the vaccine trial as quickly as possible. Ventavia was compensated by Pfizer mainly on a per-patient basis—up to a weekly limit—and rushed to enroll as many clinical trial participants as possible per week. Ventavia’s race to maximize payment and over-booking of patients resulted in sloppy and fraudulent documentation practices, poor clinical trial protocol compliance, and little oversight. Pfizer and Icon turned a blind eye to Ventavia’s misconduct, despite numerous warning signs.

Ventavia’s trial protocol and regulatory violations were so widespread, in fact, that Relator observed them on a near-daily basis during her brief employment period. For example, Relator observed:

  • fabrication and falsification of blood draw information, vital signs, signatures and other essential clinical trial data;
  • enrollment and injection of ineligible clinical trial participants, including Ventavia employees’ family members;
  • failure to timely remove ineligible patients’ data from the trial;
  • failure to maintain temperature control for the vaccine at issue;
  • failure to monitor patients after injection as required by the trial protocol;
  • principal investigator oversight failures;
  • use of unqualified and untrained personnel as vaccinators and laboratory personnel;
  • failure to maintain the “blind” as required, which is essential to the credibility and validity of the observer-blinded clinical trial;
  • ethical violations, such as failure to secure informed consent and giving patients unapproved compensation;
  • improper injection of the vaccine (i.e., by over-diluting vaccine concentrate or using the wrong needle size);
  • failure to ensure that trial site staff were properly trained as required by good clinical practices;
  • safety and confidentiality issues, including HIPAA violations; and
  • other violations of the clinical trial protocol, FDA regulations, and Federal Acquisition Regulations and their DoD supplements.

… “

 

Why should this legal action be of interest to everyone across the globe?

I’m sure that you will agree that the WHO is forcing those Covid injections across the globe as a result of the FDA original approval. In our book that needs further digging into the original authorization process.

 

Furthermore, we have grounds to believe that the WHO is currently in negotiations with countries across the planet to replace countries sovereignty with WHO directives regarding health issues.

Meaning, any psycho leading the WHO would use force to impose any health experimental drug on global citizens irrespective of those individuals’ rights and liberties granted by their countries constitutions.

(Could explain why so many countries are in the unprecedented rush to change or attempting to change their constitutions).

This in our opinion needs to be stopped.

 

This legal action could also open up another line of “Requests for Information” focused on the original clinical trials conducted by Icon, an Irish clinical research organization that has oversight of over 160 test sites worldwide.

 

We could start by identifying those 160 test sites, the subcontractors and the protocols followed.

 

Hopefully trigging some whistle blowers to disclose what has really taken place at those other trial sites, as we are of the opinion, in fact we really have difficult in believing that what has occurred at the two trial sites in this court claim in the USA are the only ones that may have grossly misrepresented the true operational shortcomings, which could include fraudulent reporting.

 

Why is this court action important?

Three reasons in our opinion

  • One: If fraud is indeed found to have taken place, then the whole authorization process can be declared null and void by a court of law.
  • Two: All contracts signed by countries for the purchase of the C “vaccines” can be automatically cancelled due to fraud.
  • Three: It will stop the genocide that is taking place across the globe, and especially it will enable the children and youth to be saved.

 

UPDATE

18 February 2022: See video: The Mainstream Media may ignore this, Wall Street is not. Moderna is down 70% from its high. Pfizer is down 19%. Blackrock Whistleblower Who Predicted The Crash of Moderna Breaks New Bombshell Information

4 March 2022: See video: Edward Dowd Explains Bombshell ‘Fraud’ Charge re Pfizer Hiding Deaths Data

 

 
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