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My name is Brook Jackson. I am a whistleblower suing Pfizer and my former employer, Ventavia Research Group, in Federal court under the False Claims Act for fraud I witnessed during the Pfizer COVID-19 MRNA clinical trials in September 2020.

I have dedicated nearly two decades of my career to ensuring the delivery of safe and effective therapeutics, vaccines, and devices to consumers. Like many others, I initially placed confidence and trust in the regulatory process and federal agencies tasked with safeguarding public health.


However, my faith was shaken when it became apparent that entities such as the U.S. Food and Drug Administration (FDA), the Center for Disease Control and Prevention (CDC), and others, have failed in their duty to protect the American people. Instead of prioritizing public health, they have chosen to cater to the interests of powerful corporations, turning a blind eye to vaccine injuries and fatalities.


In light of these failures, I believe that the path forward involves embracing transparency, exposing corruption at all levels, and holding those responsible accountable for their actions. Since September 2020, I have been tirelessly working to compile evidence for my legal team and to raise awareness about the injuries and harms stemming from mRNA COVID-19 products.


In early 2020, when the Government declared COVID-19 a pandemic, I was working as the Director of Operations for a multi-state Site Management Organization. Two of the final projects that I managed involved the testing of the cobas® SARS-CoV-2 and Abbott ID Now® RT-PCR technologies and early phase trials of Remdesivir.  


On September 8, 2020, I accepted a new position as Regional Director of Operations with a company named Ventavia Research Group. My main responsibility was to oversee the conduct of Pfizer's Phase 3 Covid-19 mRNA "vaccine" trial at several locations in Texas. 


Part of my responsibility was to ensure the rights, safety, and welfare of the people volunteering to be in the study was protected, and that the information collected from each of them was supported by the highest data integrity standards.


In the 20 years that I have been involved in clinical research, I have never seen a study conducted by an investigative site, managed by a contractor, or overseen by a pharmaceutical sponsor that scared me, until then. What I documented and reported to my former employer and to Pfizer during an internal audit was dangerous and violated Federal law. I felt that I had a responsibility to make sure that the participants were protected and that the fraudulent data being collected in the study was not used in any safety and efficacy analysis. 

On September 25, 2020, I spoke to  an agent at the FDA, and within hours, I was fired.  That moment led me to where I am today; A whistleblower who's fighting to hold those accountable for the fraud I witnessed that's now impacted hundreds of millions of lives in the United States, as well as around the world.

Listen: My Final Call with Ventavia
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